A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137633



Internal ID20704673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12690787..12691187hg38UCSC Ensembl
chr6:12691019..12691419hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405221
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137633
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00084


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