A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149440



Internal ID15881034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78927344..78962677hg38UCSC Ensembl
Innerchr17:76923426..76958759hg19UCSC Ensembl
Innerchr17:74435021..74470354hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3835334
hg1935334
hg1835334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576102
Supporting Variants
SamplesNINDS_61
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149440
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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