A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422072



Internal ID201127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37453372..37462166hg38UCSC Ensembl
chr1:37918973..37927767hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg388795
hg198795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16902035
Samples
Known GenesLINC01137
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422072
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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