A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700606



Internal ID15437258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:26449704..26455546hg38UCSC Ensembl
Innerchr4:26451326..26457168hg19UCSC Ensembl
Innerchr4:26060424..26066266hg18UCSC Ensembl
Innerchr4:26127595..26133437hg17UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg385843
hg195843
hg185843
hg175843
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515501
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700606
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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