A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664275



Internal ID9930380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14686827..14688598hg38UCSC Ensembl
Outerchr9:14686670..14688751hg38UCSC Ensembl
Innerchr9:14686825..14688596hg19UCSC Ensembl
Outerchr9:14686668..14688749hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382082
hg192082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1326e199
Supporting Variantsessv5838577, essv6419321, essv5453431, essv5625197, essv6583734, essv6378196, essv5813059, essv6039653, essv5771636, essv5813686, essv5680012, essv6079714, essv5840628, essv6106239, essv6061364, essv6566982, essv6386249, essv6326913, essv6180063, essv6439408, essv6281920, essv5406636, essv6548908, essv6251394, essv6020326, essv5781702, essv5471028, essv5557719, essv5692788
SamplesNA19703, NA19914, NA18486, NA19377, NA20356, NA19107, NA18923, NA19916, NA18916, NA18498, NA18874, NA18868, NA19172, NA20127, NA18908, NA18867, NA19451, HG01124, NA20126, NA18871, NA18907, NA18499, NA18858, NA19108, NA19467, NA19818, NA19093, NA18522, NA18487
Known GenesZDHHC21
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664275
Frequency
Sample Size1151
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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