A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926442



Internal ID22701669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101375355..101391556hg38UCSC Ensembl
chr8:102387583..102403784hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3816202
hg1916202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926442
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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