A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv971491



Internal ID16265447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:109743553..110074938hg38UCSC Ensembl
Innerchr3:109462400..109793785hg19UCSC Ensembl
Innerchr3:110945090..111276475hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38331386
hg19331386
hg18331386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591270
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)nssv971491
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