A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173588



Internal ID20740628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98946496..98946917hg38UCSC Ensembl
chr8:99958724..99959145hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423758
Supporting Variants
Samples
Known GenesOSR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173588
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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