A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925373



Internal ID22700600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6260667..6405404hg38UCSC Ensembl
chr8:6118188..6262925hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38144738
hg19144738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437367
Samples
Known GenesLOC100287015
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925373
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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