A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970105



Internal ID22745040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43926822..43926822hg38UCSC Ensembl
chr13:44500958..44500958hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387949
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970105
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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