A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3721606



Internal ID18673201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32147032..32565269hg38UCSC Ensembl
Innerchr15:32439233..32857470hg19UCSC Ensembl
Innerchr15:30226525..30644762hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38418238
hg19418238
hg18418238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036250
Supporting Variants
Samples
Known GenesCHRNA7, GOLGA8K, GOLGA8O, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3721606
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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