A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056027



Internal ID19145246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77104549..77137456hg38UCSC Ensembl
Innerchr16:77138446..77171353hg19UCSC Ensembl
Innerchr16:75695947..75728854hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3832908
hg1932908
hg1832908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559659
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)nsv1056027
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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