A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541656



Internal ID316233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113493104..113493104hg38UCSC Ensembl
chr7:113133159..113133159hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17001649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541656
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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