A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531672



Internal ID18829953
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 loss
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)nssv3531672
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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