A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031292



Internal ID21940635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71575960..71589908hg38UCSC Ensembl
chr12:71969740..71983688hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3813949
hg1913949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603630
Samples
Known GenesLGR5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031292
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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