A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442536



Internal ID21100089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89026154..89028833hg38UCSC Ensembl
chr9:91641069..91643748hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg382680
hg192680
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184205
Samples
Known GenesSHC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442536
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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