A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478795



Internal ID21136348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110144344..110144993hg38UCSC Ensembl
chr12:110582149..110582798hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996899
Samples
Known GenesIFT81
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478795
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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