A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017858



Internal ID21927201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56310199..56310332hg38UCSC Ensembl
chr8:57222758..57222891hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593200
Samples
Known GenesSDR16C5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017858
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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