A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6784905



Internal ID9842101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:44539553..44550834hg38UCSC Ensembl
Outerchr21:45959436..45970717hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3811282
hg1911282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2723673, esv2723638
Supporting Variants
SamplesSSM068
Known GenesKRTAP10-1, KRTAP10-2, TSPEAR
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6784905
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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