A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035486



Internal ID18778017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20584461..20731189hg38UCSC Ensembl
Innerchr16:20595783..20742511hg19UCSC Ensembl
Innerchr16:20503284..20650012hg18UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38146729
hg19146729
hg18146729
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2799n100
Supporting Variantsnssv3548049
Samples
Known GenesACSM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035486
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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