A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141868



Internal ID20708908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149382119..149386049hg38UCSC Ensembl
chr6:149703255..149707185hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg383931
hg193931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6607173
Supporting Variants
Samples
Known GenesTAB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141868
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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