A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18141864



Internal ID20708904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149325490..149326880hg38UCSC Ensembl
chr6:149646626..149648016hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381391
hg191391
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6614764
Supporting Variants
Samples
Known GenesTAB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18141864
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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