A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711128



Internal ID19009409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19901720hg38UCSC Ensembl
Innerchr14:19801743..20369879hg19UCSC Ensembl
Innerchr14:18871743..19439719hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38670772
hg19568137
hg18567977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043310
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)nssv3711128
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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