A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17448995



Internal ID22506865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98974263..98975044hg38UCSC Ensembl
chr8:99986491..99987272hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918522
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17448995
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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