A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526995



Internal ID18825276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18605720..19637241hg38UCSC Ensembl
Innerchr14:19382197..20105479hg19UCSC Ensembl
Innerchr14:18452197..19175240hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381031522
hg19723283
hg18723044
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040110
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, POTEG, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3526995
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