A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892474



Internal ID22667525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16075173..16080724hg38UCSC Ensembl
chr6:16075404..16080955hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385552
hg195552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420041
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892474
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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