A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004963



Internal ID21914306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114718137..114718220hg38UCSC Ensembl
chr9:117480417..117480500hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004963
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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