A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092744



Internal ID22001977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:48762035..48762035hg38UCSC Ensembl
chr12:49155818..49155818hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599213
Samples
Known GenesLINC00935
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092744
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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