A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534082



Internal ID309934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155845925..155845925hg38UCSC Ensembl
chr7:155638619..155638619hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17005943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534082
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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