A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907355



Internal ID22682562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110570476..110585315hg38UCSC Ensembl
chr6:110891679..110906518hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3814840
hg1914840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17419115
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907355
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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