A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350174



Internal ID21007727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165948301..165961200hg38UCSC Ensembl
chr2:166804811..166817710hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3812900
hg1912900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207352
Samples
Known GenesTTC21B, TTC21B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350174
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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