A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013718



Internal ID21923061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166128136..166128225hg38UCSC Ensembl
chr6:166541624..166541713hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013718
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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