A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064047



Internal ID21973280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:869715..869715hg38UCSC Ensembl
chr4:863503..863503hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553306
Samples
Known GenesGAK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064047
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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