A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047661



Internal ID19136880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42095447..42387885hg38UCSC Ensembl
Innerchr14:42564650..42857088hg19UCSC Ensembl
Innerchr14:41634400..41926838hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38292439
hg19292439
hg18292439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1885n100
Supporting Variantsnssv3530200
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)nsv1047661
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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