A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705279



Internal ID15441931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:14901981..14905311hg38UCSC Ensembl
Innerchr4:14903605..14906935hg19UCSC Ensembl
Innerchr4:14512703..14516033hg18UCSC Ensembl
Innerchr4:14579874..14583204hg17UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg383331
hg193331
hg183331
hg173331
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528647
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705279
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