A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431006



Internal ID209795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:113097541..113098774hg38UCSC Ensembl
chr1:113640163..113641396hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg381234
hg191234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16908102
Samples
Known GenesLRIG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431006
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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