A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527302



Internal ID18825583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19795860hg38UCSC Ensembl
Innerchr14:19802529..20264019hg19UCSC Ensembl
Innerchr14:18872529..19333859hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38564912
hg19461491
hg18461331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043505
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4M1, OR4Q3, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3527302
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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