A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039753



Internal ID19128972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:20453186..20489224hg38UCSC Ensembl
Innerchr16:20464508..20500546hg19UCSC Ensembl
Innerchr16:20372009..20408047hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3836039
hg1936039
hg1836039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2796n100
Supporting Variantsnssv3547116
Samples
Known GenesACSM2A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039753
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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