A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046100



Internal ID18788631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24597074..24745040hg38UCSC Ensembl
Innerchr15:24842221..24990187hg19UCSC Ensembl
Innerchr15:22393314..22541280hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38147967
hg19147967
hg18147967
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3721463
Samples
Known GenesNPAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046100
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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