A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832096



Internal ID22607031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:187470094..187472693hg38UCSC Ensembl
chr2:188334821..188337420hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481335
Samples
Known GenesTFPI
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832096
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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