A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062749



Internal ID19151968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:76573958..76670319hg38UCSC Ensembl
Innerchr16:76607855..76704216hg19UCSC Ensembl
Innerchr16:75165356..75261717hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3896362
hg1996362
hg1896362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3026n100
Supporting Variantsnssv3559646
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062749
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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