A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336645



Internal ID20994198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:176235385..176273067hg38UCSC Ensembl
chr2:177100113..177137795hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3837683
hg1937683
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208039
Samples
Known GenesMTX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336645
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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