A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837777



Internal ID22612712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158474954..158478180hg38UCSC Ensembl
chr4:159396106..159399332hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg383227
hg193227
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1607n209
Supporting Variantsnssv17493549
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837777
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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