A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17502291



Internal ID22560231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169098188..169106674hg38UCSC Ensembl
chr6:169498283..169506769hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg388487
hg198487
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5845054
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17502291
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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