A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029390



Internal ID21938733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:9062380..9062438hg38UCSC Ensembl
chr12:9214976..9215034hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598861
Samples
Known GenesLINC00612
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029390
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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