A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5481767



Internal ID259236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85212459..85213719hg38UCSC Ensembl
chr7:84841775..84843035hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg381261
hg191261
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16999487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5481767
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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