A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17504335



Internal ID22562278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23159460..23163659hg38UCSC Ensembl
chr6:23159688..23163887hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5844570
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17504335
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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