A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044961



Internal ID19134180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26365363..26387468hg38UCSC Ensembl
Innerchr14:26834569..26856674hg19UCSC Ensembl
Innerchr14:25904409..25926514hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3822106
hg1922106
hg1822106
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1855n100
Supporting Variantsnssv3528540
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044961
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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