A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900127



Internal ID22675266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26004147..26004276hg38UCSC Ensembl
chr6:26004375..26004504hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445795
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900127
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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