A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597347



Internal ID21789390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95257331..95257331hg38UCSC Ensembl
chr8:96269559..96269559hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6068502
Supporting Variants
Samples
Known GenesC8orf37
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597347
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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