A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051232



Internal ID18793763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:36449762..36783250hg38UCSC Ensembl
Innerchr15:36741963..37075451hg19UCSC Ensembl
Innerchr15:34529255..34862743hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38333489
hg19333489
hg18333489
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552234
Samples
Known GenesC15orf41
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051232
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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