A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446344



Internal ID21103897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89103800..89107007hg38UCSC Ensembl
chr9:91718715..91721922hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg383208
hg193208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195570
Samples
Known GenesSHC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446344
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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