A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897367



Internal ID22672468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81505418..81512289hg38UCSC Ensembl
chr3:81554569..81561440hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg386872
hg196872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417433
Samples
Known GenesGBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897367
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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