A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695941



Internal ID15432593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:14769495..14842781hg38UCSC Ensembl
Innerchr4:14771119..14844405hg19UCSC Ensembl
Innerchr4:14380217..14453503hg18UCSC Ensembl
Innerchr4:14447388..14520674hg17UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3873287
hg1973287
hg1873287
hg1773287
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518501
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695941
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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