A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038542



Internal ID21947885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8006927..8007002hg38UCSC Ensembl
chr12:8159523..8159598hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038542
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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