A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414028



Internal ID22471898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:141893220..141968156hg38UCSC Ensembl
chr6:142214357..142289293hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3874937
hg1974937
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900304
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414028
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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