A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046875



Internal ID19136094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:84527166..84726906hg38UCSC Ensembl
Innerchr14:84993510..85193250hg19UCSC Ensembl
Innerchr14:84063263..84263003hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38199741
hg19199741
hg18199741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532361
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)nsv1046875
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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