A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349219



Internal ID21006772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:183394232..183404488hg38UCSC Ensembl
chr2:184258960..184269216hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg3810257
hg1910257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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