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dbVar

Database of genomic structural variation

esv3676347

Organism: Homo sapiens

Study:estd217 (Besenbacher et al. 2015)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:69,261

Publication(s):Besenbacher et al. 2015

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: 2620 SVs from 96 studies. See in: genome view

Remapped(Score: Perfect):78,257,499-78,326,759

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3676347	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	78,257,499	78,326,759
esv3676347	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	78,967,216	79,036,476

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv16497916	deletion	Sequencing	de novo sequence assembly

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16497916	Remapped	Perfect	NC_000006.12:g.782 57499_78326759del6 9259	GRCh38.p12	First Pass	NC_000006.12	Chr6	78,257,499	78,326,759
essv16497916	Submitted genomic		NC_000006.11:g.789 67216_79036476del6 9259	GRCh37 (hg19)		NC_000006.11	Chr6	78,967,216	79,036,476

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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