A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087753



Internal ID21996986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8626194..8626194hg38UCSC Ensembl
chr12:8778790..8778790hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087753
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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