A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067303



Internal ID21976536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35196135..35196135hg38UCSC Ensembl
chr6:35163912..35163912hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566983
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067303
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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