A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611274



Internal ID6651493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151920609..151921591hg38UCSC Ensembl
Innerchr6:151920621..151921579hg38UCSC Ensembl
Outerchr6:151920597..151921603hg38UCSC Ensembl
chr6:152241744..152242726hg19UCSC Ensembl
Innerchr6:152241756..152242714hg19UCSC Ensembl
Outerchr6:152241732..152242738hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38983
hg19983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12585008, essv12585007, essv12585009, essv12585010
SamplesNA20514, NA19773, HG02131, NA18555
Known GenesESR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611274
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer