A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17505926



Internal ID22563871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29437967..29445341hg38UCSC Ensembl
chr8:29295484..29302858hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg387375
hg197375
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5859188
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17505926
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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