A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057053



Internal ID19146272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78943943..79014079hg38UCSC Ensembl
Innerchr16:78977840..79047976hg19UCSC Ensembl
Innerchr16:77535341..77605477hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3870137
hg1970137
hg1870137
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559763
Samples
Known GenesWWOX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057053
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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