A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065697



Internal ID19154916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35236333..35496532hg38UCSC Ensembl
Innerchr16:34470704..34730903hg19UCSC Ensembl
Innerchr16:34328205..34588404hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38260200
hg19260200
hg18260200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3722471
Samples
Known GenesLOC146481, LOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065697
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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