A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711124



Internal ID19009405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19806180hg38UCSC Ensembl
Innerchr14:19801743..20274339hg19UCSC Ensembl
Innerchr14:18871743..19344179hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38575232
hg19472597
hg18472437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041089
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)nssv3711124
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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