A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142639



Internal ID20709679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38516873..38517539hg38UCSC Ensembl
chr6:38484649..38485315hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405320
Supporting Variants
Samples
Known GenesBTBD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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