A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904658



Internal ID22679836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106376516..106381487hg38UCSC Ensembl
chr6:106824391..106829362hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384972
hg194972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412903
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904658
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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