A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6772676



Internal ID9831879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:87975788..87975946hg38UCSC Ensembl
Outerchr16:88009394..88009552hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2714947, esv2714946
Supporting Variants
SamplesSSM065
Known GenesBANP
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)essv6772676
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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