A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712133



Internal ID18663728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20880514..20934425hg38UCSC Ensembl
Innerchr14:21348673..21402584hg19UCSC Ensembl
Innerchr14:20418513..20472424hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3853912
hg1953912
hg1853912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040201
Supporting Variants
Samples
Known GenesECRP, RNASE3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712133
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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