A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347288



Internal ID21004841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:220472701..220473822hg38UCSC Ensembl
chr2:221337422..221338543hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381122
hg191122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086174
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347288
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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