A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046900



Internal ID19136119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:47943836..47968850hg38UCSC Ensembl
Innerchr14:48413039..48438053hg19UCSC Ensembl
Innerchr14:47482789..47507803hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3825015
hg1925015
hg1825015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530984
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)nsv1046900
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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