A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559985



Internal ID18858266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88382623..88423727hg38UCSC Ensembl
Innerchr16:88449031..88490135hg19UCSC Ensembl
Innerchr16:86976532..87017636hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3841105
hg1941105
hg1841105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057561
Supporting Variants
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)nssv3559985
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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