A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5916735



Internal ID22691954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163258941..163261853hg38UCSC Ensembl
chr6:163679973..163682885hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg382913
hg192913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410579
Samples
Known GenesPACRG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5916735
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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