A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027687



Internal ID21937030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30796076..30796164hg38UCSC Ensembl
chr12:30949010..30949098hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607360
Samples
Known GenesLINC00941
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027687
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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