A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6025653



Internal ID21934996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:18760825..18760899hg38UCSC Ensembl
chr12:18913759..18913833hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6025653
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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