A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17501048



Internal ID22558985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107058481..107060680hg38UCSC Ensembl
chr6:107379685..107381884hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5843977
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17501048
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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