A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062080



Internal ID18804611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:90007677..90096340hg38UCSC Ensembl
Innerchr16:90074085..90162748hg19UCSC Ensembl
Innerchr16:88601586..88690249hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3888664
hg1988664
hg1888664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719128
Samples
Known GenesC16orf3, DBNDD1, GAS8, PRDM7, URAHP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062080
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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