A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350314



Internal ID21007867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98906560..98931841hg38UCSC Ensembl
chr2:99523023..99548304hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3825282
hg1925282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208844
Samples
Known GenesKIAA1211L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350314
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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