A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419661



Internal ID22477531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163359943..163359943hg38UCSC Ensembl
chr6:163780975..163780975hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38242
hg19242
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947603
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419661
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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