A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026497



Internal ID21935840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57873746..57873845hg38UCSC Ensembl
chr12:58267529..58267628hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026497
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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