A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139724



Internal ID20706764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132483276..132483995hg38UCSC Ensembl
chr6:132804415..132805134hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38720
hg19720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610707
Supporting Variants
Samples
Known GenesSTX7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139724
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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