A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510167



Internal ID22568117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:87649599..87652506hg38UCSC Ensembl
chr8:88661827..88664734hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg382908
hg192908
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852877
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510167
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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