A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3738092



Internal ID18689687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68917..523947hg38UCSC Ensembl
Innerchr4:68809..517736hg19UCSC Ensembl
Innerchr4:58809..507736hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38455031
hg19448928
hg18448928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001899
Supporting Variants
Samples
Known GenesABCA11P, PIGG, ZNF141, ZNF595, ZNF718, ZNF721, ZNF732, ZNF876P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3738092
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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