A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534235



Internal ID216948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46017685..46017685hg38UCSC Ensembl
chr7:46057284..46057284hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16995248
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534235
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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