A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736099



Internal ID20512044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61237787..61237929hg38UCSC Ensembl
chr8:62150346..62150488hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269977
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736099
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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