A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832634



Internal ID22607569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36964639..36974365hg38UCSC Ensembl
chr2:37191782..37201508hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg389727
hg199727
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484787
Samples
Known GenesSTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832634
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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