A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711127



Internal ID19009408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19886834hg38UCSC Ensembl
Innerchr14:19801743..20354993hg19UCSC Ensembl
Innerchr14:18871743..19424833hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38655886
hg19553251
hg18553091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052324
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4K2, 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)nssv3711127
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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