A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5453831



Internal ID231942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227778388..227778446hg38UCSC Ensembl
chr1:227966089..227966147hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16897466
Samples
Known GenesSNAP47
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5453831
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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