A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6953922



Internal ID10058328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:413715..413870hg38UCSC Ensembl
Outerchr17:263506..263661hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2715302, esv2715301
Supporting Variants
SamplesSSM025
Known GenesC17orf97
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)essv6953922
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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