A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027625



Internal ID21936968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25928116..25928214hg38UCSC Ensembl
chr12:26081049..26081147hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027625
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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