A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026137



Internal ID21935480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124986968..124987050hg38UCSC Ensembl
chr12:125471514..125471596hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600525
Samples
Known GenesDHX37
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026137
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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