A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531028



Internal ID18829309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:55926860..55957075hg38UCSC Ensembl
Innerchr14:56393578..56423793hg19UCSC Ensembl
Innerchr14:55463331..55493546hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3830216
hg1930216
hg1830216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043948
Supporting Variants
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)nssv3531028
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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