A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449578



Internal ID21107131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124848436..124854757hg38UCSC Ensembl
chr9:127610715..127617036hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg386322
hg196322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176628
Samples
Known GenesWDR38
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449578
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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