A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343045



Internal ID21000598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:209072260..209079972hg38UCSC Ensembl
chr2:209936984..209944696hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg387713
hg197713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4274n223
Supporting Variantsnssv18085013
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343045
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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