A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477877



Internal ID255443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93812487..93812825hg38UCSC Ensembl
chr9:96574769..96575107hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477877
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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