A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142708



Internal ID20709748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39811106..39826364hg38UCSC Ensembl
chr6:39778882..39794140hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3815259
hg1915259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399153
Supporting Variants
Samples
Known GenesDAAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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