A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350292



Internal ID21007845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113958301..113959400hg38UCSC Ensembl
chr2:114715878..114716977hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075613
Samples
Known GenesACTR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350292
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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