A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077647



Internal ID21986880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37698242..37698242hg38UCSC Ensembl
chr6:37666018..37666018hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576719
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077647
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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