A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908861



Internal ID22684071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92319900..92322983hg38UCSC Ensembl
chr10:94079657..94082740hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg383084
hg193084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354833
Samples
Known GenesMARCH5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908861
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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