A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711136



Internal ID19009417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19922383hg38UCSC Ensembl
Innerchr14:19802529..20390542hg19UCSC Ensembl
Innerchr14:18872529..19460382hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38691435
hg19588014
hg18587854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046179
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4K2, OR4K5, OR4M1, OR4N2, 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)nssv3711136
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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