A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2716419



Internal ID10300055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:80981161..80981621hg38UCSC Ensembl
Outerchr17:78954961..78955421hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38461
hg19461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6925056, essv6920998, essv6696348, essv6971616, essv6678551, essv6843222, essv6725226, essv6832020
SamplesSSM045, SSM028, SSM084, SSM018, SSM017, SSM032, SSM081, SSM037
Known Genes
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)esv2716419
Frequency
Sample Size96
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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