A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063955



Internal ID18806486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69994778..70105639hg38UCSC Ensembl
Innerchr16:70028681..70139542hg19UCSC Ensembl
Innerchr16:68586182..68697043hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38110862
hg19110862
hg18110862
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3002n100
Supporting Variantsnssv3559483, nssv3559484, nssv3559485
Samples
Known GenesMIR1972-1, MIR1972-2, PDXDC2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063955
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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