A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3532223



Internal ID18830504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22162256..22473159hg38UCSC Ensembl
Innerchr14:22630152..22942149hg19UCSC Ensembl
Innerchr14:21699992..22011989hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38310904
hg19311998
hg18311998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053889
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)nssv3532223
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