A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639495



Internal ID18937776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:131595882..131625067hg38UCSC Ensembl
Innerchr4:132517037..132546222hg19UCSC Ensembl
Innerchr4:132736487..132765672hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3829186
hg1929186
hg1829186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016741
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)nssv3639495
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