A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091305



Internal ID22000538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:26849580..26849580hg38UCSC Ensembl
chr12:27002513..27002513hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg382785
hg192785
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609852
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091305
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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