A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3636139



Internal ID18934420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:156046811..156063549hg38UCSC Ensembl
Innerchr4:156967963..156984701hg19UCSC Ensembl
Innerchr4:157187413..157204151hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3816739
hg1916739
hg1816739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026377
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3636139
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