A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347407



Internal ID21004960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42817673..42818464hg38UCSC Ensembl
chr2:43044813..43045604hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38792
hg19792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347407
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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