A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575925



Internal ID16363334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68112848..68173906hg38UCSC Ensembl
Innerchr17:66108989..66170047hg19UCSC Ensembl
Innerchr17:63620627..63681642hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3861059
hg1961059
hg1861016
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5756n54
Supporting Variantsnssv875906, nssv875907
Samples
Known GenesLINC00674
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575925
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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