A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832697



Internal ID22607632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206696592..206701986hg38UCSC Ensembl
chr2:207561316..207566710hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg385395
hg195395
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482027
Samples
Known GenesDYTN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832697
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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