A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12177298



Internal ID6878308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2613870..2615978hg38UCSC Ensembl
Innerchr6:2613896..2615953hg38UCSC Ensembl
Outerchr6:2613845..2616004hg38UCSC Ensembl
chr6:2614104..2616212hg19UCSC Ensembl
Innerchr6:2614130..2616187hg19UCSC Ensembl
Outerchr6:2614079..2616238hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382109
hg192109
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3607911
Supporting Variants
SamplesNA21100
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12177298
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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