A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575987



Internal ID16016710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73339121..73361671hg38UCSC Ensembl
Innerchr17:71335260..71357810hg19UCSC Ensembl
Innerchr17:68846855..68869405hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3822551
hg1922551
hg1822551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149803
SamplesHGDP00553
Known GenesSDK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575987
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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