A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653792



Internal ID15390444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156385014..156385628hg38UCSC Ensembl
Innerchr4:157306166..157306780hg19UCSC Ensembl
Innerchr4:157525616..157526230hg18UCSC Ensembl
Innerchr4:157663771..157664385hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38615
hg19615
hg18615
hg17615
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517773
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653792
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer