A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17507435



Internal ID22565383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:56135744..56145404hg38UCSC Ensembl
chr8:57048303..57057963hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg389661
hg199661
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5863156
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17507435
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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