A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064080



Internal ID19153299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:68151257..68204774hg38UCSC Ensembl
Innerchr16:68185160..68238677hg19UCSC Ensembl
Innerchr16:66742661..66796178hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3853518
hg1953518
hg1853518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2996n100
Supporting Variantsnssv3559444, nssv3559443
Samples
Known GenesNFATC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064080
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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