A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017264



Internal ID21926607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88959369..88959460hg38UCSC Ensembl
chr9:91574284..91574375hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580273
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017264
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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