A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580824



Internal ID21772867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102080221..102080221hg38UCSC Ensembl
chr8:103092449..103092449hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070400
Supporting Variants
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580824
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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