A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050113



Internal ID19139332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9134675..9201485hg38UCSC Ensembl
Innerchr16:9228532..9295342hg19UCSC Ensembl
Innerchr16:9136033..9202843hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3866811
hg1966811
hg1866811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557118
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050113
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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