A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502504



Internal ID22560445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158924882..158927372hg38UCSC Ensembl
chr6:159345914..159348404hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382491
hg192491
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844415
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502504
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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