A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892032



Internal ID22667077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140287108..140287445hg38UCSC Ensembl
chr4:141208262..141208599hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418166
Samples
Known GenesLOC100129858, SCOC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892032
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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