A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677695



Internal ID9943800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93049591..93050382hg38UCSC Ensembl
chr9:95811873..95812664hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38792
hg19792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6189062, essv5448577, essv6086125, essv6511801, essv5991707, essv6204111, essv6273836, essv6573355, essv6181112, essv6044105, essv6538091, essv6112681, essv6219721, essv5978856, essv6564943, essv6341997, essv6091873, essv6545102, essv6365232, essv5667361, essv6129363, essv6237503, essv5839729, essv5990713, essv6018848, essv6485897, essv5907643
SamplesNA18486, NA19920, NA19379, NA19384, NA19130, NA19917, NA19372, NA19371, NA19471, NA19317, NA19456, NA19327, NA19114, NA18856, NA19452, NA19395, NA19625, NA18961, NA19256, NA19311, NA19248, NA19713, NA18873, NA19116, NA19711, NA19430, NA19129
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677695
Frequency
Sample Size1151
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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