A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423599



Internal ID22481469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120625198..120625198hg38UCSC Ensembl
chr6:120946344..120946344hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5964222
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423599
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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