A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713391



Internal ID19011672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18605720..19265122hg38UCSC Ensembl
Innerchr14:19382197..19852821hg19UCSC Ensembl
Innerchr14:18452197..18922821hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38659403
hg19470625
hg18470625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047182
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, POTEG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713391
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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