A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459654



Internal ID21117207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:38511485..38602806hg38UCSC Ensembl
chr12:38905287..38996608hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3891322
hg1991322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998640
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459654
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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