A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670634



Internal ID15407286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:66820154..66822277hg38UCSC Ensembl
Innerchr5:66115982..66118105hg19UCSC Ensembl
Innerchr5:66151738..66153861hg18UCSC Ensembl
Innerchr5:66151738..66153861hg17UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg382124
hg192124
hg182124
hg172124
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516753
Supporting Variants
Samples
Known GenesMAST4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670634
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