A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449424



Internal ID22507294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55965564..56039265hg38UCSC Ensembl
chr6:55830362..55904063hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3873702
hg1973702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898253
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449424
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002


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