A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908128



Internal ID22683338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80585384..80587204hg38UCSC Ensembl
chr10:82345140..82346960hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg381821
hg191821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359142
Samples
Known GenesSH2D4B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908128
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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