A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010961



Internal ID21920304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91132640..91132732hg38UCSC Ensembl
chr9:93894922..93895014hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587225
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010961
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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