A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060619



Internal ID19149838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77656299..77709861hg38UCSC Ensembl
Innerchr16:77690196..77743758hg19UCSC Ensembl
Innerchr16:76247697..76301259hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3853563
hg1953563
hg1853563
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3030n100
Supporting Variantsnssv3719062
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)nsv1060619
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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