A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442115



Internal ID21099668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96770901..96771900hg38UCSC Ensembl
chr9:99533183..99534182hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189565
Samples
Known GenesZNF510
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442115
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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