A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918708



Internal ID22693930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:83225313..83239653hg38UCSC Ensembl
chr8:84137548..84151888hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3814341
hg1914341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438479
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918708
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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