A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17509179



Internal ID22567129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36408725..36411643hg38UCSC Ensembl
chr8:36266243..36269161hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382919
hg192919
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854496
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17509179
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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