A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5475761



Internal ID253395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19822520..19822659hg38UCSC Ensembl
chr8:19680031..19680170hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009107
Samples
Known GenesINTS10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5475761
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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