A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673952



Internal ID15410604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134001210..134255550hg38UCSC Ensembl
Innerchr4:134922365..135176705hg19UCSC Ensembl
Innerchr4:135141815..135396155hg18UCSC Ensembl
Innerchr4:135279970..135534310hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38254341
hg19254341
hg18254341
hg17254341
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520680
Supporting Variants
Samples
Known GenesPABPC4L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673952
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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