A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528313



Internal ID18826594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18661498..19265122hg38UCSC Ensembl
Innerchr14:19437975..19852821hg19UCSC Ensembl
Innerchr14:18507975..18922821hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38603625
hg19414847
hg18414847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039323
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, POTEG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3528313
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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