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dbVar

Database of genomic structural variation

nsv3169199

Organism: Homo sapiens

Study:nstd158 (Cleal et al. 2019)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:53,314

Publication(s):Cleal et al. 2019

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: 421 SVs from 37 studies. See in: genome view

Remapped(Score: Perfect):28,607,056-28,660,375

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3169199	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	28,607,059 (-3, +3)	28,660,372 (-3, +3)
nsv3169199	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	28,464,576 (-3, +3)	28,517,889 (-3, +3)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv14239982	inversion	DB115	Sequencing	Paired-end mapping	36

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14239982	Remapped	Perfect	NC_000008.11:g.(28 607056_28607062)_( 28660369_28660375) inv186	GRCh38.p12	First Pass	NC_000008.11	Chr8	28,607,059 (-3, +3)	28,660,372 (-3, +3)
nssv14239982	Submitted genomic		NC_000008.10:g.(28 464573_28464579)_( 28517886_28517892) inv186	GRCh37 (hg19)		NC_000008.10	Chr8	28,464,576 (-3, +3)	28,517,889 (-3, +3)

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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