A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051891



Internal ID18794422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32507614hg38UCSC Ensembl
Innerchr15:32458661..32799815hg19UCSC Ensembl
Innerchr15:30245953..30587107hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38341155
hg19341155
hg18341155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2542n100
Supporting Variantsnssv3721611
Samples
Known GenesCHRNA7, GOLGA8K, GOLGA8O, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051891
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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