A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449299



Internal ID21106852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93220347..93222680hg38UCSC Ensembl
chr9:95982629..95984962hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382334
hg192334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178398
Samples
Known GenesWNK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449299
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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