A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148574



Internal ID15854706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43337104..43778538hg38UCSC Ensembl
Innerchr14:43806307..44247741hg19UCSC Ensembl
Innerchr14:42876057..43317491hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38441435
hg19441435
hg18441435
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564634
Supporting Variants
Samples1780862300_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148574
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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