A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530971



Internal ID18829252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47762752..47808236hg38UCSC Ensembl
Innerchr14:48231955..48277439hg19UCSC Ensembl
Innerchr14:47301705..47347189hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3845485
hg1945485
hg1845485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054615
Supporting Variants
Samples
Known GenesLINC00648
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3530971
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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