A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149356



Internal ID15876582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:34843464..34890183hg38UCSC Ensembl
Innerchr17:33170483..33217202hg19UCSC Ensembl
Innerchr17:30194596..30241315hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3846720
hg1946720
hg1846720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574740
Supporting Variants
SamplesHGDP00864
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149356
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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