A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500991



Internal ID22558928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120679319..120690787hg38UCSC Ensembl
chr6:121000465..121011933hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3811469
hg1911469
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844248
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500991
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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