A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530925



Internal ID18829206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19746329hg38UCSC Ensembl
Innerchr14:19790343..20214488hg19UCSC Ensembl
Innerchr14:18860343..19284328hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38515381
hg19424146
hg18423986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044000
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3530925
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer