A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528591



Internal ID18826872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:33066718..33119859hg38UCSC Ensembl
Innerchr14:33535924..33589065hg19UCSC Ensembl
Innerchr14:32605675..32658816hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3853142
hg1953142
hg1853142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037356
Supporting Variants
Samples
Known GenesNPAS3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3528591
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