A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151841



Internal ID15880370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8779046..8816277hg38UCSC Ensembl
Innerchr3:8820732..8857963hg19UCSC Ensembl
Innerchr3:8795732..8832963hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3837232
hg1937232
hg1837232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589621
Supporting Variants
SamplesNINDS_200
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151841
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