A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607926



Internal ID6994857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3242030..3243855hg38UCSC Ensembl
Innerchr6:3242031..3243854hg38UCSC Ensembl
Outerchr6:3242029..3243856hg38UCSC Ensembl
chr6:3242264..3244089hg19UCSC Ensembl
Innerchr6:3242265..3244088hg19UCSC Ensembl
Outerchr6:3242263..3244090hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381826
hg191826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12179111, essv12179110, essv12179107, essv12179109, essv12179108
SamplesNA19141, NA19917, HG02946, HG03267, HG03202
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607926
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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