A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563615



Internal ID16351024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18624804..19849588hg38UCSC Ensembl
Innerchr14:19401281..20317747hg19UCSC Ensembl
Innerchr14:18471281..19387587hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381224785
hg19916467
hg18916307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3494n54
Supporting Variantsnssv821330
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H2, OR4M1, OR4N2, OR4Q3, POTEG, POTEM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563615
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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