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dbVar

Database of genomic structural variation

nsv5014086

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:97,538

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

Submitted genomic80,147,023-80,244,563

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5014086	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	80,147,025 (-2)	80,244,562 (-1, +1)
nsv5014086	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	78,120,824 (-2)	78,218,361 (-1, +1)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16575691	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16575691	Submitted genomic		NC_000017.11:g.(80 147023_?)_(8024456 1_80244563)dup	GRCh38 (hg38)		NC_000017.11	Chr17	80,147,025 (-2)	80,244,562 (-1, +1)
nssv16575691	Remapped	Perfect	NC_000017.10:g.(78 120822_?)_(7821836 0_78218362)dup	GRCh37.p13	First Pass	NC_000017.10	Chr17	78,120,824 (-2)	78,218,361 (-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)
nssv16575691	<0.001	1	29246

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