A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574499



Internal ID16015222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16768138..16814681hg38UCSC Ensembl
Innerchr17:16671452..16717995hg19UCSC Ensembl
Innerchr17:16612177..16658720hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3846544
hg1946544
hg1846544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5477n54
Supporting Variantsnssv868806
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)nsv574499
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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