A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035372



Internal ID18777903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..19169707hg38UCSC Ensembl
Innerchr14:19002112..19801743hg19UCSC Ensembl
Innerchr14:18072112..18871743hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38944073
hg19799632
hg18799632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1751n100
Supporting Variantsnssv3526836
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, POTEG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035372
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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