A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046934



Internal ID19136153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27385529..27486050hg38UCSC Ensembl
Innerchr14:27854735..27955256hg19UCSC Ensembl
Innerchr14:26924575..27025096hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38100522
hg19100522
hg18100522
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3712271
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)nsv1046934
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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