A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927199



Internal ID22702427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27711911..27712631hg38UCSC Ensembl
chr8:27569428..27570148hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38721
hg19721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437788
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927199
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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