A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528526



Internal ID18480121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24458107..24524460hg38UCSC Ensembl
Innerchr14:24927313..24993666hg19UCSC Ensembl
Innerchr14:23997153..24063506hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3866354
hg1966354
hg1866354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039955
Supporting Variants
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)nssv3528526
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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