A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060575



Internal ID19149794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:63488443..63628178hg38UCSC Ensembl
Innerchr16:63522347..63662082hg19UCSC Ensembl
Innerchr16:62079848..62219583hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38139736
hg19139736
hg18139736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559386
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)nsv1060575
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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