A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473513



Internal ID21131066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:16065222..16139330hg38UCSC Ensembl
chr12:16218156..16292264hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3874109
hg1974109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997662
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473513
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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