A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18147635



Internal ID20714675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99460001..99460900hg38UCSC Ensembl
chr6:99907877..99908776hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610836
Supporting Variants
Samples
Known GenesUSP45
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18147635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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