A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059725



Internal ID19148944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80857434..80876934hg38UCSC Ensembl
Innerchr16:80891331..80910831hg19UCSC Ensembl
Innerchr16:79448832..79468332hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3819501
hg1919501
hg1819501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719079
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)nsv1059725
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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