A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895521



Internal ID22670605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102045644..102129174hg38UCSC Ensembl
chr3:101764488..101848018hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg3883531
hg1983531
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402224
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895521
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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