A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505818



Internal ID22563762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44876461..44882208hg38UCSC Ensembl
chr6:44844198..44849945hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg385748
hg195748
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845614
Supporting Variants
Samples
Known GenesSUPT3H
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505818
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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