A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449579



Internal ID21107132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92071161..92077616hg38UCSC Ensembl
chr9:94833443..94839898hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg386456
hg196456
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195142
Samples
Known GenesSPTLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449579
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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