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dbVar

Database of genomic structural variation

nsv4406730

Organism: Homo sapiens

Study:nstd174 (DGV Gold Standard)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:368,914

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 1194 SVs from 99 studies. See in: genome view

Remapped(Score: Perfect):143,512,169-143,881,082

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv4406730	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	143,512,169	143,512,169	143,881,082	143,881,082
nsv4406730	Remapped	Pass	GRCh38.p12	PATCHES	Second Pass	NW_018654714.1	Chr7\|NW_01 8654714.1	131,533	131,533	425,306	425,306
nsv4406730	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	143,209,262	143,215,528	143,528,214	143,578,175

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15712721	copy number gain	Multiple	Multiple

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv15712721	Remapped	Pass	NW_018654714.1:g.( 131533_131533)_(42 5306_425306)dup	GRCh38.p12	Second Pass	NW_018654714.1	Chr7\|NW_01 8654714.1	131,533	131,533	425,306	425,306
nssv15712721	Remapped	Perfect	NC_000007.14:g.(14 3512169_143512169) _(143881082_143881 082)dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	143,512,169	143,512,169	143,881,082	143,881,082
nssv15712721	Submitted genomic		NC_000007.13:g.(14 3209262_143215528) _(143528214_143578 175)dup	GRCh37 (hg19)		NC_000007.13	Chr7	143,209,262	143,215,528	143,528,214	143,578,175

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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