A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925137



Internal ID22700364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28798147..28800381hg38UCSC Ensembl
chr8:28655664..28657898hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg382235
hg192235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446260
Samples
Known GenesINTS9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925137
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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