A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17418122



Internal ID22475992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143121395..143121395hg38UCSC Ensembl
chr6:143442532..143442532hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5948838
Supporting Variants
Samples
Known GenesAIG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17418122
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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