A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574503



Internal ID16015226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16768138..16821302hg38UCSC Ensembl
Innerchr17:16671452..16724616hg19UCSC Ensembl
Innerchr17:16612177..16665341hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3853165
hg1953165
hg1853165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5477n54
Supporting Variantsnssv868814, nssv868818, nssv868815, nssv868816, nssv868817
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)nsv574503
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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