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dbVar

Database of genomic structural variation

nsv5030527

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:181,683

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: 639 SVs from 58 studies. See in: genome view

Submitted genomic60,554,638-60,736,323

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5030527	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	60,554,639 (-1, +1)	60,736,321 (-2, +2)
nsv5030527	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	60,588,543 (-1, +1)	60,770,225 (-2, +2)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16576691	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16576691	Submitted genomic		NC_000016.10:g.(60 554638_60554640)_( 60736319_60736323) inv	GRCh38 (hg38)		NC_000016.10	Chr16	60,554,639 (-1, +1)	60,736,321 (-2, +2)
nssv16576691	Remapped	Perfect	NC_000016.9:g.(605 88542_60588544)_(6 0770223_60770227)i nv	GRCh37.p13	First Pass	NC_000016.9	Chr16	60,588,543 (-1, +1)	60,770,225 (-2, +2)

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)
nssv16576691	<0.001	2	29246

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