A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18144162



Internal ID20711202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45291179..45306036hg38UCSC Ensembl
chr6:45258916..45273773hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3814858
hg1914858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405447
Supporting Variants
Samples
Known GenesSUPT3H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18144162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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