A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024431



Internal ID21933774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110172879..110173051hg38UCSC Ensembl
chr12:110610684..110610856hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615566
Samples
Known GenesIFT81
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024431
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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