A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094519



Internal ID22003752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25370437..25370437hg38UCSC Ensembl
chr12:25523371..25523371hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094519
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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