A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666970



Internal ID9933075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3656600..3656807hg38UCSC Ensembl
chr9:3656600..3656807hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6462544, essv6115264, essv6493128, essv5853593, essv5822825, essv6031109, essv5569659, essv5712900, essv5975558, essv5622890, essv5433894, essv6597325, essv5405177, essv6237800, essv6148268, essv5970260, essv5446450, essv5787251, essv5734604, essv6112850, essv5974756, essv6415810, essv5957197, essv5519205, essv6450489, essv6242892, essv6241835, essv6055611, essv6483553, essv5731078, essv6595641, essv6371116
SamplesHG01441, NA20766, NA18861, NA10851, NA19399, NA19092, HG00115, NA20768, NA19189, NA19789, HG01136, NA12342, NA19391, NA19655, NA18626, NA19469, NA19401, NA19147, NA19434, NA20804, NA19380, NA19324, NA19311, NA19360, NA20582, NA19474, HG00123, NA19770, NA19213, NA19900, NA19129, NA19429
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666970
Frequency
Sample Size1151
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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