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dbVar

Database of genomic structural variation

esv4009084

Organism: Homo sapiens

Study:estd231 (Wong et al. 2017)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:57,950

Publication(s):Wong et al. 2017

Links to Other Resources

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: 474 SVs from 53 studies. See in: genome view

Remapped(Score: Perfect):147,003,934-147,061,883

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv4009084	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	147,003,934	147,061,883
esv4009084	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	146,701,026	146,758,975

Variant Call Information

Variant Call ID	Type	Method	Analysis	Subject Phenotype
essv26065476	inversion	Sequencing	Split read and paired-end mapping	Juvenile idiopathic arthritis

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv26065476	Remapped	Perfect	NC_000007.14:g.147 003934_147061883in v	GRCh38.p12	First Pass	NC_000007.14	Chr7	147,003,934	147,061,883
essv26065476	Submitted genomic		NC_000007.13:g.146 701026_146758975in v	GRCh37 (hg19)		NC_000007.13	Chr7	146,701,026	146,758,975

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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