A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169970



Internal ID21314031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9105179..9125030hg38UCSC Ensembl
Outerchr16:9105130..9128386hg38UCSC Ensembl
Innerchr16:9199036..9218887hg19UCSC Ensembl
Outerchr16:9198987..9222243hg19UCSC Ensembl
Innerchr16:9106537..9126388hg18UCSC Ensembl
Outerchr16:9106488..9129744hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3823257
hg1923257
hg1823257
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14241745
SamplesNGO_24
Known GenesC16orf72
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169970
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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