A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582597



Internal ID21774640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94590903..94590954hg38UCSC Ensembl
chr8:95603131..95603182hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019329
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582597
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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