A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094329



Internal ID22003562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95798912..95798912hg38UCSC Ensembl
chr12:96192690..96192690hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611704
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094329
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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