A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893762



Internal ID22668827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43787617..43787917hg38UCSC Ensembl
chr6:43755354..43755654hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893762
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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