A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141606



Internal ID20708646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153293987..153307443hg38UCSC Ensembl
chr6:153615122..153628578hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3813457
hg1913457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617996
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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