A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891017



Internal ID22666049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134341058..134341365hg38UCSC Ensembl
chr6:134662196..134662503hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411063
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891017
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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