A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047956



Internal ID19137175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22185576..22486728hg38UCSC Ensembl
Innerchr14:22653472..22955716hg19UCSC Ensembl
Innerchr14:21723312..22025556hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38301153
hg19302245
hg18302245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1806n100
Supporting Variantsnssv3532244
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)nsv1047956
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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