A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871911



Internal ID22646849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33859906..33862821hg38UCSC Ensembl
chr1:34325507..34328422hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg382916
hg192916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378089
Samples
Known GenesCSMD2, HMGB4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871911
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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