A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916715



Internal ID22691934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102526163..102538779hg38UCSC Ensembl
chr8:103538391..103551007hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3812617
hg1912617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440700
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916715
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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