A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18139165



Internal ID20706205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154497177..154502676hg38UCSC Ensembl
chr6:154818311..154823810hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610479
Supporting Variants
Samples
Known GenesCNKSR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18139165
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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