A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045732



Internal ID18788263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24444802..24550111hg38UCSC Ensembl
Innerchr14:24914008..25019317hg19UCSC Ensembl
Innerchr14:23983848..24089157hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38105310
hg19105310
hg18105310
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3712268
Samples
Known GenesCMA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045732
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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