A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457341



Internal ID21114894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27935291..27936180hg38UCSC Ensembl
chr12:28088224..28089113hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38890
hg19890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000115
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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