A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411706



Internal ID22469576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163628684..163628684hg38UCSC Ensembl
chr6:164049716..164049716hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967451
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411706
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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