A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12387660



Internal ID6922617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:61597404..61606059hg38UCSC Ensembl
Innerchr6:61597412..61606052hg38UCSC Ensembl
Outerchr6:61597397..61606067hg38UCSC Ensembl
chr6:62307309..62315964hg19UCSC Ensembl
Innerchr6:62307317..62315957hg19UCSC Ensembl
Outerchr6:62307302..62315972hg19UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg388656
hg198656
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3609208
Supporting Variants
SamplesNA21118
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12387660
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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