A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17500927



Internal ID22558864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111449954..111451980hg38UCSC Ensembl
chr6:111771157..111773183hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382027
hg192027
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844310
Supporting Variants
Samples
Known GenesREV3L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17500927
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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