A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336095



Internal ID20993648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:73268901..73270900hg38UCSC Ensembl
chr2:73496029..73498028hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089710
Samples
Known GenesFBXO41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336095
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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