A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998511



Internal ID19158047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:75259597..75473167hg38UCSC Ensembl
Innerchr4:76184807..76398377hg19UCSC Ensembl
Innerchr4:76403831..76617401hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38213571
hg19213571
hg18213571
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633828
Samples
Known GenesLOC441025
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998511
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