A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071139



Internal ID21980372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24504528..24504528hg38UCSC Ensembl
chr4:24506151..24506151hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537673
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071139
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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