A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834213



Internal ID22609148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:96500125..96501924hg38UCSC Ensembl
chr2:97165862..97167661hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482967
Samples
Known GenesNEURL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834213
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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