A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023487



Internal ID21932830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56470194..56470917hg38UCSC Ensembl
chr12:56863978..56864701hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg38724
hg19724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602883
Samples
Known GenesSPRYD4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023487
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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