A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574502



Internal ID16015225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16768138..16817315hg38UCSC Ensembl
Innerchr17:16671452..16720629hg19UCSC Ensembl
Innerchr17:16612177..16661354hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3849178
hg1949178
hg1849178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5477n54
Supporting Variantsnssv868813, nssv868812
Samples
Known GenesCCDC144A, FAM106CP, USP32P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574502
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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