A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610829



Internal ID6997746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132054051..132057854hg38UCSC Ensembl
Innerchr6:132054051..132057854hg38UCSC Ensembl
Outerchr6:132053949..132057988hg38UCSC Ensembl
chr6:132375191..132378994hg19UCSC Ensembl
Innerchr6:132375191..132378994hg19UCSC Ensembl
Outerchr6:132375089..132379128hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg383804
hg193804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12553374, essv12553373, essv12553375
SamplesNA12878, HG00376, NA11892
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610829
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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