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dbVar

Database of genomic structural variation

nsv4905824

Organism: Homo sapiens

Study:nstd200 (Abel et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:279,409

Publication(s):Abel et al. 2020

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: 867 SVs from 62 studies. See in: genome view

Submitted genomic103,328,115-103,607,526

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4905824	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	103,328,117 (-2)	103,607,525 (-1, +1)
nsv4905824	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	102,583,045 (-2)	102,862,453 (-1, +1)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16593677	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16593677	Submitted genomic		NC_000023.11:g.(10 3328115_?)_(103607 524_103607526)dup	GRCh38 (hg38)		NC_000023.11	ChrX	103,328,117 (-2)	103,607,525 (-1, +1)
nssv16593677	Remapped	Perfect	NC_000023.10:g.(10 2583043_?)_(102862 452_102862454)dup	GRCh37.p13	First Pass	NC_000023.10	ChrX	102,583,045 (-2)	102,862,453 (-1, +1)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16593677	<0.001	2	29246

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