A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073257



Internal ID21982490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101470621..101470621hg38UCSC Ensembl
chr4:102391778..102391778hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553532
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073257
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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