A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv977357



Internal ID16271313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162136930..162238888hg38UCSC Ensembl
Innerchr3:161854718..161956676hg19UCSC Ensembl
Innerchr3:163337412..163439370hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38101959
hg19101959
hg18101959
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592148
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv977357
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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