A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530991



Internal ID18829272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48219532..48257681hg38UCSC Ensembl
Innerchr14:48688735..48726884hg19UCSC Ensembl
Innerchr14:47758485..47796634hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3838150
hg1938150
hg1838150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037219
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3530991
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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