A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926762



Internal ID22701989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98446132..98446181hg38UCSC Ensembl
chr10:100205889..100205938hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354123
Samples
Known GenesHPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926762
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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