A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531690



Internal ID18829971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47762752..47808073hg38UCSC Ensembl
Innerchr14:48231955..48277276hg19UCSC Ensembl
Innerchr14:47301705..47347026hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3845322
hg1945322
hg1845322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041310
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)nssv3531690
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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