A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837195



Internal ID22612130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95063528..95068164hg38UCSC Ensembl
chr3:94782372..94787008hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg384637
hg194637
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837195
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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