A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17985844



Internal ID20552884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:99044220..99054631hg38UCSC Ensembl
chr10:100803977..100814388hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3810412
hg1910412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453864
Supporting Variants
Samples
Known GenesHPSE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17985844
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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