A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6143627



Internal ID342828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:13605010..13605090hg38UCSC Ensembl
chr12:13757944..13758024hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17054210
Samples
Known GenesGRIN2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6143627
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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