A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037997



Internal ID21947340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9065153..9065246hg38UCSC Ensembl
chr12:9217749..9217842hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17616324
Samples
Known GenesA2M-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037997
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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