A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895765



Internal ID22670851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173935854..173935929hg38UCSC Ensembl
chr2:174800582..174800657hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17393863
Samples
Known GenesSP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895765
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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