A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085835



Internal ID21995068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:47759993..47759993hg38UCSC Ensembl
chr12:48153776..48153776hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602913
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085835
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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