A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137809



Internal ID20704849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:129139336..129240657hg38UCSC Ensembl
chr6:129460481..129561802hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38101322
hg19101322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603889
Supporting Variants
Samples
Known GenesLAMA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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