Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

esv3674662

Organism: Homo sapiens

Study:estd217 (Besenbacher et al. 2015)
Variant Type:sequence alteration
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:3,380

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: 96 SVs from 25 studies. See in: genome view

Remapped(Score: Perfect):23,969,086-23,972,465

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3674662	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	23,969,086	23,972,465
esv3674662	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	24,295,576	24,298,955

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv16496400	sequence alteration	Sequencing	de novo sequence assembly

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16496400	Remapped	Perfect	GRCh38.p12	First Pass	NC_000001.11	Chr1	23,969,086	23,972,465
essv16496400	Submitted genomic		GRCh37 (hg19)		NC_000001.10	Chr1	24,295,576	24,298,955

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

You are here: NCBI