A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070714



Internal ID21979947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166969861..166969861hg38UCSC Ensembl
chr6:167383349..167383349hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070714
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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