A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897314



Internal ID22672415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77571314..77571389hg38UCSC Ensembl
chr3:77620465..77620540hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415850
Samples
Known GenesROBO2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897314
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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