A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6009618



Internal ID9862528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:75532543..75556739hg38UCSC Ensembl
Outerchr6:75532386..75556905hg38UCSC Ensembl
Innerchr6:76242259..76266455hg19UCSC Ensembl
Outerchr6:76242102..76266621hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3824520
hg1924520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659482
Supporting Variants
SamplesNA20533
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6009618
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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