A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068361



Internal ID21977594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:56797210..56797210hg38UCSC Ensembl
chr4:57663376..57663376hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549678
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068361
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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