A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506155



Internal ID22564101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121606545..121610090hg38UCSC Ensembl
chr8:122618785..122622330hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg383546
hg193546
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853879
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506155
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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