A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353258



Internal ID21010811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176203210..176289410hg38UCSC Ensembl
chr2:177067938..177154138hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3886201
hg1986201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208038
Samples
Known GenesMTX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353258
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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