A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440081



Internal ID21097634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98761901..98763900hg38UCSC Ensembl
chr9:101524183..101526182hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191724
Samples
Known GenesANKS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440081
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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