A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095466



Internal ID22004699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10718386..10718386hg38UCSC Ensembl
chr12:10870985..10870985hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607265
Samples
Known GenesYBX3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095466
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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