A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059399



Internal ID19148618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:62989713..63013930hg38UCSC Ensembl
Innerchr16:63023617..63047834hg19UCSC Ensembl
Innerchr16:61581118..61605335hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3824218
hg1924218
hg1824218
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3722722
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)nsv1059399
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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