A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531000



Internal ID18829281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48319210..48435916hg38UCSC Ensembl
Innerchr14:48788413..48905119hg19UCSC Ensembl
Innerchr14:47858163..47974869hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38116707
hg19116707
hg18116707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048456
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531000
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