A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059503



Internal ID19148722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77638145..77707683hg38UCSC Ensembl
Innerchr16:77672042..77741580hg19UCSC Ensembl
Innerchr16:76229543..76299081hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3869539
hg1969539
hg1869539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3030n100
Supporting Variantsnssv3559667
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)nsv1059503
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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