A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17369338



Internal ID22595007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98940174..99191923hg38UCSC Ensembl
chr10:100699931..100951680hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38251750
hg19251750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5926200
Supporting Variants
Samples
Known GenesHPSE2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17369338
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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