A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044092



Internal ID18786623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32166460..32550909hg38UCSC Ensembl
Innerchr15:32458661..32843110hg19UCSC Ensembl
Innerchr15:30245953..30630402hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38384450
hg19384450
hg18384450
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2538n100
Supporting Variantsnssv3721612
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)nsv1044092
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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