A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027394



Internal ID21936737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25071010..25085992hg38UCSC Ensembl
chr12:25223944..25238926hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3814983
hg1914983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612231
Samples
Known GenesLRMP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027394
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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