A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5479915



Internal ID257429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32470741..32473266hg38UCSC Ensembl
chr7:32510353..32512878hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg382526
hg192526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5479915
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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