A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574494



Internal ID16015217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:16491769..16495241hg38UCSC Ensembl
Innerchr17:16395083..16398555hg19UCSC Ensembl
Innerchr17:16335808..16339280hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg383473
hg193473
hg183473
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv868800
Samples
Known GenesFAM211A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574494
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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