A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033848



Internal ID21943191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:42961242..42997825hg38UCSC Ensembl
chr12:43355045..43391628hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3836584
hg1936584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033848
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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