A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892843



Internal ID22667899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22466002..22472538hg38UCSC Ensembl
chr4:22467625..22474161hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg386537
hg196537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428308
Samples
Known GenesGPR125
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892843
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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