A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478371



Internal ID255930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26550325..26564116hg38UCSC Ensembl
chr7:26589944..26603735hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3813792
hg1913792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16994978
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478371
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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