A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3636036



Internal ID18934317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:144003421..144098631hg38UCSC Ensembl
Innerchr4:144924574..145019784hg19UCSC Ensembl
Innerchr4:145144024..145239234hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3895211
hg1995211
hg1895211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016258
Supporting Variants
Samples
Known GenesGYPB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3636036
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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