A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896997



Internal ID22672094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114006815..114015200hg38UCSC Ensembl
chr6:114327979..114336364hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg388386
hg198386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896997
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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