A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3746287



Internal ID19044568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7238099..7257261hg38UCSC Ensembl
Innerchr5:7238212..7257374hg19UCSC Ensembl
Innerchr5:7291212..7310374hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3819163
hg1919163
hg1819163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016432
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)nssv3746287
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