A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603889



Internal ID20976960
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 StatusM
Merged Variants
Supporting Variantsnssv18137809
Samples
Known GenesLAMA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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