A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421729



Internal ID22479599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13847465..13856724hg38UCSC Ensembl
chr6:13847696..13856955hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg389260
hg199260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5896297
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421729
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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