A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882200



Internal ID22657177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23334339..23335069hg38UCSC Ensembl
chr1:23660832..23661562hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17368927
Samples
Known GenesHNRNPR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882200
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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