A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908788



Internal ID22683998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92344226..92347004hg38UCSC Ensembl
chr10:94103983..94106761hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg382779
hg192779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361804
Samples
Known GenesMARCH5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908788
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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