A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035714



Internal ID19124933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46340067..46448876hg38UCSC Ensembl
Innerchr14:46809270..46918079hg19UCSC Ensembl
Innerchr14:45879020..45987829hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38108810
hg19108810
hg18108810
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531657
Samples
Known GenesLINC00871
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035714
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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