A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677319



Internal ID9943424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:71986668..71990379hg38UCSC Ensembl
Outerchr9:71986511..71990533hg38UCSC Ensembl
Innerchr9:74601584..74605295hg19UCSC Ensembl
Outerchr9:74601427..74605449hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg384023
hg194023
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6169299
SamplesNA19661
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677319
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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