A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575929



Internal ID16016652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68910076..68927570hg38UCSC Ensembl
Innerchr17:66906217..66923711hg19UCSC Ensembl
Innerchr17:64417812..64435306hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3817495
hg1917495
hg1817495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875910
Samples
Known GenesABCA8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575929
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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