A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169986



Internal ID21314047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54042113..54046035hg38UCSC Ensembl
Outerchr20:54042112..54049104hg38UCSC Ensembl
Innerchr20:52658652..52662574hg19UCSC Ensembl
Outerchr20:52658651..52665643hg19UCSC Ensembl
Innerchr20:52092059..52095981hg18UCSC Ensembl
Outerchr20:52092058..52099050hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg386993
hg196993
hg186993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250644
SamplesMLY_5
Known GenesBCAS1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169986
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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