A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713472



Internal ID19011753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46465971..46527104hg38UCSC Ensembl
Innerchr14:46935174..46996307hg19UCSC Ensembl
Innerchr14:46004924..46066057hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3861134
hg1961134
hg1861134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051025
Supporting Variants
Samples
Known GenesLINC00871
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713472
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer