A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051599



Internal ID18794130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32612463hg38UCSC Ensembl
Innerchr15:32458661..32904664hg19UCSC Ensembl
Innerchr15:30245953..30691956hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38446004
hg19446004
hg18446004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2538n100
Supporting Variantsnssv3721628
Samples
Known GenesCHRNA7, GOLGA8K, GOLGA8O, GOLGA8R, 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)nsv1051599
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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