A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507434



Internal ID22565382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56093370..56094469hg38UCSC Ensembl
chr8:57005929..57007028hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5856540
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507434
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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