A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140199



Internal ID20707239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143040001..143042400hg38UCSC Ensembl
chr6:143361138..143363537hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615122
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140199
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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