A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3626539



Internal ID18924820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:63255703..63428054hg38UCSC Ensembl
Innerchr4:64121421..64293772hg19UCSC Ensembl
Innerchr4:63804016..63976367hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38172352
hg19172352
hg18172352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012882
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)nssv3626539
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