A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6765546



Internal ID9825095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:1118014..1118276hg38UCSC Ensembl
Outerchr10:1163954..1164216hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2729439
Supporting Variants
SamplesSSM063
Known GenesWDR37
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)essv6765546
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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