A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339745



Internal ID20997298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113961301..113962400hg38UCSC Ensembl
chr2:114718878..114719977hg19UCSC 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 Variantsnssv18075614
Samples
Known GenesACTR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339745
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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