A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995831



Internal ID21905174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173208704..173210847hg38UCSC Ensembl
chr4:174129855..174131998hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg382144
hg192144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552726
Samples
Known GenesGALNT7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995831
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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