A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462831



Internal ID21120384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41358583..41359113hg38UCSC Ensembl
chr12:41752385..41752915hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38531
hg19531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000878
Samples
Known GenesPDZRN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462831
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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