A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv976519



Internal ID16270475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:149550714..149551571hg38UCSC Ensembl
Innerchr3:149268501..149269358hg19UCSC Ensembl
Innerchr3:150751191..150752048hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38858
hg19858
hg18858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592009
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)nssv976519
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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