A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17580918



Internal ID21772961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99838977..99839149hg38UCSC Ensembl
chr10:101598734..101598906hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001924
Supporting Variants
Samples
Known GenesABCC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17580918
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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