A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500901



Internal ID22558838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108757512..108762036hg38UCSC Ensembl
chr6:109078715..109083239hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384525
hg194525
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844210
Supporting Variants
Samples
Known GenesLINC00222
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500901
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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