A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096293



Internal ID22005526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101735871..101735871hg38UCSC Ensembl
chr12:102129649..102129649hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598855
Samples
Known GenesSYCP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096293
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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