A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046680



Internal ID19135899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35139141..35196168hg38UCSC Ensembl
Innerchr14:35608347..35665374hg19UCSC Ensembl
Innerchr14:34678098..34735125hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3857028
hg1957028
hg1857028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3712280
Samples
Known GenesKIAA0391
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046680
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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