A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575933



Internal ID16363342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:69157245..69219571hg38UCSC Ensembl
Innerchr17:67153386..67215712hg19UCSC Ensembl
Innerchr17:64664981..64727307hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3862327
hg1962327
hg1862327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5757n54
Supporting Variantsnssv875913
Samples
Known GenesABCA10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575933
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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