A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070000



Internal ID21979233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25491964..25491964hg38UCSC Ensembl
chr4:25493586..25493586hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38625
hg19625
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545775
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070000
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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