A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5477n54



Internal ID20138901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16757407..16821302hg38UCSC Ensembl
chr17:16660721..16724616hg19UCSC Ensembl
chr17:16601446..16665341hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3863896
hg1963896
hg1863896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574499, nsv574497, nsv574501, nsv574502, nsv574500, nsv574495, nsv574496, nsv574503, nsv574498
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)dgv5477n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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