A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv976617



Internal ID16270573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149551336..149552125hg38UCSC Ensembl
Innerchr3:149269123..149269912hg19UCSC Ensembl
Innerchr3:150751813..150752602hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38790
hg19790
hg18790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592024
Supporting Variants
Samples
Known GenesWWTR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv976617
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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