A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639646



Internal ID18937927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7963347..7989546hg38UCSC Ensembl
Innerchr5:7963460..7989659hg19UCSC Ensembl
Innerchr5:8016460..8042659hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3826200
hg1926200
hg1826200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027319
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)nssv3639646
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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