A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738595



Internal ID20514565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123233107..123233199hg38UCSC Ensembl
chr10:124992623..124992715hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293456
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738595
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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