A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575924



Internal ID16363333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68112848..68167654hg38UCSC Ensembl
Innerchr17:66108989..66163795hg19UCSC Ensembl
Innerchr17:63620627..63675390hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3854807
hg1954807
hg1854764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5756n54
Supporting Variantsnssv875905
Samples
Known GenesLINC00674
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575924
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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