A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217082



Internal ID20784122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149407003..149483630hg38UCSC Ensembl
chr6:149728139..149804766hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3876628
hg1976628
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600205
Supporting Variants
Samples
Known GenesTAB2, ZC3H12D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217082
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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