A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv873119



Internal ID16167075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:48816711..48829811hg38UCSC Ensembl
Innerchr17:46894073..46907173hg19UCSC Ensembl
Innerchr17:44249072..44262172hg18UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3813101
hg1913101
hg1813101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575485
Supporting Variants
Samples
Known GenesTTLL6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv873119
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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