A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6762691



Internal ID9824436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:104812956..104815930hg38UCSC Ensembl
Outerchr6:105260831..105263805hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg382975
hg192975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2732531
Supporting Variants
SamplesSSM062
Known GenesHACE1
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)essv6762691
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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