A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043617



Internal ID19132836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19758610hg38UCSC Ensembl
Innerchr14:19802529..20226769hg19UCSC Ensembl
Innerchr14:18872529..19296609hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38527662
hg19424241
hg18424081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1767n100
Supporting Variantsnssv3527292, nssv3527293
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, 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)nsv1043617
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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