A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149702



Internal ID15854066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36609563..36634759hg38UCSC Ensembl
Innerchr17:34965999..34991217hg19UCSC Ensembl
Innerchr17:32040112..32065330hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3825197
hg1925219
hg1825219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574915
Supporting Variants
Samples1780854556_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149702
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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