A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732920



Internal ID20508846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17408102..17408426hg38UCSC Ensembl
chr8:17265611..17265935hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279721
Samples
Known GenesMTMR7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732920
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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