A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971022



Internal ID22745957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26559795..26559795hg38UCSC Ensembl
chr13:27133932..27133932hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389381
Samples
Known GenesWASF3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971022
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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