A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036467



Internal ID19125686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38444425..38465671hg38UCSC Ensembl
Innerchr14:38913629..38934875hg19UCSC Ensembl
Innerchr14:37983380..38004626hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3821247
hg1921247
hg1821247
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1872n100
Supporting Variantsnssv3528637
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)nsv1036467
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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