A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082194



Internal ID21991427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:76873916..76873916hg38UCSC Ensembl
chr12:77267696..77267696hg19UCSC Ensembl
Cytoband12q21.2
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611516
Samples
Known GenesCSRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082194
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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