A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610282



Internal ID6997199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106670920..106681417hg38UCSC Ensembl
Innerchr6:106670933..106681404hg38UCSC Ensembl
Outerchr6:106670907..106681430hg38UCSC Ensembl
chr6:107118795..107129292hg19UCSC Ensembl
Innerchr6:107118808..107129279hg19UCSC Ensembl
Outerchr6:107118782..107129305hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3810498
hg1910498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12498981, essv12498983, essv12498982, essv12498984
SamplesHG02072, NA18639, HG01859, HG02084
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610282
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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