A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663859



Internal ID9929964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113700868..113701073hg38UCSC Ensembl
chr9:116463148..116463353hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5997399, essv6433781, essv6164160, essv5915809, essv5464937, essv5548875, essv5522925, essv5753400, essv6223657, essv5828957, essv6154554, essv5869746, essv5584709, essv6494374, essv6128128, essv6251409, essv6220878, essv5636197, essv5574615, essv6550790, essv6326252, essv6042707, essv6100039, essv6263624, essv6134115, essv5814148, essv5938616, essv5652893, essv5784025, essv6472550, essv6482615, essv6421472, essv6043529, essv6241713, essv6172226, essv6217967, essv5909147, essv6084924, essv5650748, essv5683906, essv5589238, essv6362930, essv5472417, essv5564756, essv5425148, essv5468958
SamplesHG01060, NA11830, HG00143, NA18507, HG00315, NA19819, HG00737, HG00115, NA12399, NA20589, HG01351, NA20769, NA18916, NA11918, NA20540, HG00334, HG00281, NA20759, NA12282, HG01069, NA18868, HG01072, NA19385, NA19901, NA18520, NA20515, NA11993, NA20536, NA12043, NA19375, NA18961, HG00375, NA07037, NA12763, NA06986, HG00123, NA20510, NA20807, HG00280, HG01251, HG00274, NA19430, NA18488, NA20322, NA12006, NA18511
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663859
Frequency
Sample Size1151
Observed Gain0
Observed Loss46
Observed Complex0
Frequencyn/a


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