A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3529892



Internal ID18828173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106016244..106635772hg38UCSC Ensembl
Innerchr14:106482116..107091777hg19UCSC Ensembl
Innerchr14:105553161..106162822hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38619529
hg19609662
hg18609662
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054822
Supporting Variants
Samples
Known GenesLINC00221, LINC00226
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3529892
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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