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dbVar

Database of genomic structural variation

nsv4953198

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:62,954

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: 1105 SVs from 82 studies. See in: genome view

Submitted genomic906,479-969,569

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4953198	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	906,543 (-64, +3)	969,496 (-2, +73)
nsv4953198	Remapped	Good	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	946,180 (-64, +3)	1,009,132 (-2, +73)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16493429	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16493429	Submitted genomic		NC_000007.14:g.(90 6479_906546)_(9694 94_969569)dup	GRCh38 (hg38)		NC_000007.14	Chr7	906,543 (-64, +3)	969,496 (-2, +73)
nssv16493429	Remapped	Good	NC_000007.13:g.(94 6116_946183)_(1009 130_1009205)dup	GRCh37.p13	First Pass	NC_000007.13	Chr7	946,180 (-64, +3)	1,009,132 (-2, +73)

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)
nssv16493429	<0.001	1	29246

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