A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834161



Internal ID22609096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97671993..97673521hg38UCSC Ensembl
chr2:98288456..98289984hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg381529
hg191529
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483060, nssv17483061
Samples
Known GenesLINC01125
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834161
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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