A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458564



Internal ID21116117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:38682701..38687200hg38UCSC Ensembl
chr12:39076503..39081002hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998666
Samples
Known GenesCPNE8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458564
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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