A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5553078



Internal ID326361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136789025..136789060hg38UCSC Ensembl
chr7:136473772..136473807hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17002770
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5553078
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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