A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5538953



Internal ID313969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151140577..151140577hg38UCSC Ensembl
chr5:150520138..150520138hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16975747
Samples
Known GenesANXA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5538953
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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