A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670835



Internal ID9936940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:77337938..77338064hg38UCSC Ensembl
Outerchr6:77337781..77338217hg38UCSC Ensembl
Innerchr6:78047655..78047781hg19UCSC Ensembl
Outerchr6:78047498..78047934hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6134660, essv5686011, essv6135954, essv6079983, essv6075929, essv6327989, essv5412657, essv5670369, essv6009110
SamplesNA19394, NA19448, NA18868, NA19901, NA19462, NA18871, NA19401, NA19129, NA19463
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670835
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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