A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015097



Internal ID21924440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54235323..54252628hg38UCSC Ensembl
chr6:54100121..54117426hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3817306
hg1917306
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573884
Samples
Known GenesMLIP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015097
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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