A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031106



Internal ID21940449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56718552..56718620hg38UCSC Ensembl
chr12:57112336..57112404hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610775
Samples
Known GenesNACA
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031106
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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