A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921927



Internal ID22697151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48895637..48896597hg38UCSC Ensembl
chr8:49808196..49809156hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38961
hg19961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921927
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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