A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060109



Internal ID19149328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32081501..32632041hg38UCSC Ensembl
Innerchr16:32092822..32643362hg19UCSC Ensembl
Innerchr16:32000323..32550863hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38550541
hg19550541
hg18550541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2850n100
Supporting Variantsnssv3549379
Samples
Known GenesHERC2P4, LOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060109
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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