A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17506208



Internal ID22564154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124735101..124736800hg38UCSC Ensembl
chr8:125747343..125749042hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5848127
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17506208
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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