A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924315



Internal ID22699542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10751703..10757466hg38UCSC Ensembl
chr8:10609213..10614976hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg385764
hg195764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430154
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924315
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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