A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962961



Internal ID22737897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43531656..43531656hg38UCSC Ensembl
chr5:43531758..43531758hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417650
Samples
Known GenesPAIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962961
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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