A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074019



Internal ID21983252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87010204..87010204hg38UCSC Ensembl
chr6:87719922..87719922hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570176
Samples
Known GenesHTR1E
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074019
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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