A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902313



Internal ID22677470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71830794..71832851hg38UCSC Ensembl
chr6:72540497..72542554hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg382058
hg192058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442373
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902313
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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