A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712284



Internal ID19010565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38481411..38564740hg38UCSC Ensembl
Innerchr14:38950615..39033944hg19UCSC Ensembl
Innerchr14:38020366..38103695hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3883330
hg1983330
hg1883330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038162
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)nssv3712284
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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