A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv959677



Internal ID16253633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:16197487..16199512hg38UCSC Ensembl
Innerchr3:16238994..16241019hg19UCSC Ensembl
Innerchr3:16213998..16216023hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382026
hg192026
hg182026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589816
Supporting Variants
Samples
Known GenesGALNT15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv959677
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