A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142667



Internal ID20709707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39099901..39105100hg38UCSC Ensembl
chr6:39067677..39072876hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407775
Supporting Variants
Samples
Known GenesSAYSD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142667
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00601


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