A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6439408



Internal ID9808770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14686827..14688598hg38UCSC Ensembl
Outerchr9:14686670..14688751hg38UCSC Ensembl
Innerchr9:14686825..14688596hg19UCSC Ensembl
Outerchr9:14686668..14688749hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382082
hg192082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664275
Supporting Variants
SamplesNA19914
Known GenesZDHHC21
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6439408
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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