A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5839033



Internal ID22613968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44958093..44978716hg38UCSC Ensembl
chr4:44960110..44980733hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3820624
hg1920624
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5839033
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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