A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427548



Internal ID22485418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168264320..168264320hg38UCSC Ensembl
chr6:168665000..168665000hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5956515
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427548
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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