A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3626521



Internal ID18924802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62511213..62547001hg38UCSC Ensembl
Innerchr4:63376931..63412719hg19UCSC Ensembl
Innerchr4:63059526..63095314hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3835789
hg1935789
hg1835789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002195
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)nssv3626521
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