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dbVar

Database of genomic structural variation

nsv832871

Organism: Homo sapiens

Study:nstd68 (Wong et al. 2006)
Variant Type:copy number variation
Method Type:BAC aCGH
Submitted on:NCBI35 (hg17)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:227,962

Publication(s):Wong et al. 2006

Links to Other Resources

Overlapping Genes

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: 605 SVs from 52 studies. See in: genome view

Remapped(Score: Perfect):99,215,657-99,443,618

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv832871	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	99,215,657	99,443,618
nsv832871	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	99,681,994	99,909,955
nsv832871	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000014.7	Chr14	98,751,747	98,979,708

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv1451148	copy number gain	BAC aCGH	Probe signal intensity

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv1451148	Remapped	Perfect	NC_000014.9:g.(992 15657_?)_(?_994436 18)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	99,215,657	99,443,618
nssv1451148	Remapped	Perfect	NC_000014.8:g.(996 81994_?)_(?_999099 55)dup	GRCh37.p13	First Pass	NC_000014.8	Chr14	99,681,994	99,909,955
nssv1451148	Submitted genomic		NC_000014.7:g.(987 51747_?)_(?_989797 08)dup	NCBI35 (hg17)		NC_000014.7	Chr14	98,751,747	98,979,708

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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