A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908058



Internal ID22683268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102107993..102108720hg38UCSC Ensembl
chr8:103120221..103120948hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444381
Samples
Known GenesNCALD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908058
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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