A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047190



Internal ID19136409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44822776..44848100hg38UCSC Ensembl
Innerchr14:45291979..45317303hg19UCSC Ensembl
Innerchr14:44361729..44387053hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3825325
hg1925325
hg1825325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530436
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)nsv1047190
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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