A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17421288



Internal ID22479158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131555399..131557644hg38UCSC Ensembl
chr6:131876539..131878784hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg382246
hg192246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5904013
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17421288
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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