A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422617



Internal ID201658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7915359..7918194hg38UCSC Ensembl
chr1:7975419..7978254hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg382836
hg192836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17683927
Samples
Known GenesTNFRSF9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422617
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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