A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151752



Internal ID15881288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21215817..21303734hg38UCSC Ensembl
Innerchr3:21257309..21345226hg19UCSC Ensembl
Innerchr3:21232313..21320230hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3887918
hg1987918
hg1887918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589888
Supporting Variants
SamplesNINDS_96
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151752
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