A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149357



Internal ID15528622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35282228..35364390hg38UCSC Ensembl
Innerchr17:33609247..33691409hg19UCSC Ensembl
Innerchr17:30633360..30715522hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3882163
hg1982163
hg1882163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574742
Supporting Variants
SamplesHGDP00667
Known GenesSLFN11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149357
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer