A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420416



Internal ID199520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9597093..9597266hg38UCSC Ensembl
chr1:9657151..9657324hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16890346
Samples
Known GenesTMEM201
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420416
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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