A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348207



Internal ID21005760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46627575..46628241hg38UCSC Ensembl
chr2:46854714..46855380hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090569
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348207
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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