A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575932



Internal ID16016655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:69153832..69331665hg38UCSC Ensembl
Innerchr17:67149973..67327806hg19UCSC Ensembl
Innerchr17:64661568..64839401hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38177834
hg19177834
hg18177834
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875912
Samples
Known GenesABCA10, ABCA5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575932
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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