A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574312



Internal ID16361721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6169149..6227773hg38UCSC Ensembl
Innerchr17:6072469..6131093hg19UCSC Ensembl
Innerchr17:6013193..6071817hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3858625
hg1958625
hg1858625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149685
SamplesHGDP01201
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574312
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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