A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059906



Internal ID18802437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88683753..88838113hg38UCSC Ensembl
Innerchr16:88750161..88904521hg19UCSC Ensembl
Innerchr16:87277662..87432022hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38154361
hg19154361
hg18154361
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3064n100
Supporting Variantsnssv3559991
Samples
Known GenesAPRT, CDT1, CTU2, GALNS, LOC100289580, MIR4722, PIEZO1, RNF166, SNAI3, SNAI3-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059906
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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