A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140439



Internal ID20707480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:141431631..141437333hg38UCSC Ensembl
chr6:141752768..141758470hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg385703
hg195703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617085
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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