A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039739



Internal ID19128958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:86576619..86662418hg38UCSC Ensembl
Innerchr14:87042963..87128762hg19UCSC Ensembl
Innerchr14:86112716..86198515hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3885800
hg1985800
hg1885800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532551
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)nsv1039739
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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