A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039256



Internal ID18781787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6608311..6638066hg38UCSC Ensembl
Innerchr16:6658312..6688067hg19UCSC Ensembl
Innerchr16:6598313..6628068hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3829756
hg1929756
hg1829756
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2704n100
Supporting Variantsnssv3557038, nssv3557041, nssv3557039, nssv3718849, nssv3557040, nssv3718848, nssv3557035, nssv3718847, nssv3557036, nssv3557037
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039256
Frequency
Sample Size29084
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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