A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5896638



Internal ID22671733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183449645..183449714hg38UCSC Ensembl
chr3:183167433..183167502hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17409980
Samples
Known GenesLINC00888
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5896638
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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