A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057561



Internal ID19146780
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 StatusM
Merged Variants
Supporting Variantsnssv3559985
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)nsv1057561
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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