A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528600



Internal ID18480195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34417750..34505568hg38UCSC Ensembl
Innerchr14:34886956..34974774hg19UCSC Ensembl
Innerchr14:33956707..34044525hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3887819
hg1987819
hg1887819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048369
Supporting Variants
Samples
Known GenesSPTSSA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3528600
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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