A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043823



Internal ID19133042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54176280..54240787hg38UCSC Ensembl
Innerchr15:54468477..54532985hg19UCSC Ensembl
Innerchr15:52255769..52320277hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3864508
hg1964509
hg1864509
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552434
Samples
Known GenesUNC13C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043823
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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