A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575940



Internal ID16363349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:70207774..70225876hg38UCSC Ensembl
Innerchr17:68203915..68222017hg19UCSC Ensembl
Innerchr17:65715510..65733612hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3818103
hg1918103
hg1818103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149795
SamplesHGDP01304
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575940
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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