A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1014326



Internal ID16308282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:171455069..171573082hg38UCSC Ensembl
Innerchr4:172376220..172494233hg19UCSC Ensembl
Innerchr4:172612795..172730808hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38118014
hg19118014
hg18118014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596185
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1014326
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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