A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038516



Internal ID21947859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45038612..45038693hg38UCSC Ensembl
chr12:45432395..45432476hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598796
Samples
Known GenesDBX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038516
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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