A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6694196



Internal ID9762065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:73208923..73223697hg38UCSC Ensembl
Outerchr6:73918646..73933420hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3814775
hg1914775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2732285
Supporting Variants
SamplesSSM037
Known GenesKHDC1L
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)essv6694196
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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