A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663019



Internal ID9582438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112550065..112550268hg38UCSC Ensembl
chr9:115312345..115312548hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6158645, essv5870145, essv5405568, essv6520763, essv6266837, essv6483409, essv6247272, essv6450564, essv6005825
SamplesNA19445, NA19625, HG01055, NA19379, NA19474, NA19383, NA19716, NA19318, NA19099
Known GenesKIAA1958
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663019
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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