A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923877



Internal ID22699104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85093074..85093370hg38UCSC Ensembl
chr8:86005309..86005605hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923877
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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