A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837024



Internal ID22611959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73911430..73921079hg38UCSC Ensembl
chr3:73960581..73970230hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg389650
hg199650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494777
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837024
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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