A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981466



Internal ID55012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45179648..45195448hg38UCSC Ensembl
chr6:45147385..45163185hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3815801
hg1915801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463974
Supporting Variants
Samples
Known GenesSUPT3H
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981466
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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