A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv976755



Internal ID16270711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:150762859..150763449hg38UCSC Ensembl
Innerchr3:150480646..150481236hg19UCSC Ensembl
Innerchr3:151963336..151963926hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38591
hg19591
hg18591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592042
Supporting Variants
Samples
Known GenesSIAH2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv976755
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