A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6035116



Internal ID21944459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119290011..119290414hg38UCSC Ensembl
chr12:119727816..119728219hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603626
Samples
Known GenesLINC00934
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6035116
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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