A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610686



Internal ID6997603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125385339..125389779hg38UCSC Ensembl
Innerchr6:125385400..125389719hg38UCSC Ensembl
Outerchr6:125385279..125389840hg38UCSC Ensembl
chr6:125706485..125710925hg19UCSC Ensembl
Innerchr6:125706546..125710865hg19UCSC Ensembl
Outerchr6:125706425..125710986hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384441
hg194441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12537191, essv12537192, essv12537189, essv12537190
SamplesNA20531, HG01682, HG01459, HG01464
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610686
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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