A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420037



Internal ID199153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36426788..36427063hg38UCSC Ensembl
chr1:36892389..36892664hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16901444
Samples
Known GenesOSCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420037
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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