A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345497



Internal ID21003050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28869631..28872095hg38UCSC Ensembl
chr2:29092497..29094961hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg382465
hg192465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088138
Samples
Known GenesTRMT61B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345497
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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