A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714573



Internal ID19012854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20376297..20909084hg38UCSC Ensembl
Innerchr15:20581550..21114413hg19UCSC Ensembl
Innerchr15:18841564..19379038hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38532788
hg19532864
hg18537475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036968
Supporting Variants
Samples
Known GenesCXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3714573
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