A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064660



Internal ID21973893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43983721..43983721hg38UCSC Ensembl
chr4:43985738..43985738hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552902
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064660
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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