A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486101



Internal ID263475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94685869..94686431hg38UCSC Ensembl
chr7:94315181..94315743hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16999668
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486101
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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