A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17510069



Internal ID22568019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84154532..84156031hg38UCSC Ensembl
chr8:85066767..85068266hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5857420
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17510069
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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