A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574496



Internal ID16015219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16757407..16815401hg38UCSC Ensembl
Innerchr17:16660721..16718715hg19UCSC Ensembl
Innerchr17:16601446..16659440hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3857995
hg1957995
hg1857995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5477n54
Supporting Variantsnssv868802, nssv868803
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)nsv574496
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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