A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662702



Internal ID9928807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89471690..89471814hg38UCSC Ensembl
chr9:92086605..92086729hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6149271, essv6038165, essv6493954, essv6318792, essv6156423, essv6032411, essv5910891, essv6321740, essv6522973, essv5473575, essv5724407, essv5436368, essv6583665, essv5891781, essv6159806, essv6518195, essv6281760, essv5642498, essv5649605, essv5652701, essv5577019, essv5475546, essv6158275, essv5998135, essv5964864, essv5872087, essv6415295, essv5892845, essv6115337, essv5766195, essv5660086, essv5534921, essv5528867, essv6193973, essv5875458, essv6344679
SamplesHG00442, HG00249, HG01188, HG00315, NA18530, HG00449, HG00261, HG00327, HG00138, HG01365, HG01069, HG00253, HG01353, HG00543, HG00313, HG00137, HG00154, HG00344, HG00275, NA18572, HG01390, HG00324, HG00331, HG00321, HG01334, HG00254, HG00278, HG01375, HG00418, HG00125, HG00513, HG00342, HG00310, HG01082, NA18612, NA18620
Known GenesSEMA4D
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662702
Frequency
Sample Size1151
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


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