A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv970922



Internal ID16264878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103163097..103232017hg38UCSC Ensembl
Innerchr3:102881941..102950861hg19UCSC Ensembl
Innerchr3:104364631..104433551hg18UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3868921
hg1968921
hg1868921
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591193
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)nssv970922
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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