A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038926



Internal ID19128145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18559262..19169707hg38UCSC Ensembl
Innerchr14:19335739..19801743hg19UCSC Ensembl
Innerchr14:18405739..18871743hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38610446
hg19466005
hg18466005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1758n100
Supporting Variantsnssv3526945
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)nsv1038926
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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