A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138748



Internal ID20705788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:126424914..126426515hg38UCSC Ensembl
chr6:126746060..126747661hg19UCSC Ensembl
Cytoband6q22.32
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617372
Supporting Variants
Samples
Known GenesCENPW
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138748
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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