A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17420041



Internal ID22477911
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 StatusS
Merged Variantsnsv5892474
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17420041
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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