A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501147



Internal ID22559084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125606925..125608959hg38UCSC Ensembl
chr6:125928071..125930105hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg382035
hg192035
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843737
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501147
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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