A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575460



Internal ID16362869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46771550..46772216hg38UCSC Ensembl
Innerchr17:44848916..44849582hg19UCSC Ensembl
Innerchr17:42204084..42204745hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38667
hg19667
hg18662
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv873062, nssv873061
Samples
Known GenesWNT3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575460
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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