A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338650



Internal ID20996203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97638834..97660499hg38UCSC Ensembl
chr2:98255297..98276962hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3821666
hg1921666
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208835
Samples
Known GenesACTR1B, COX5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338650
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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