A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052904



Internal ID21962137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102093648..102093648hg38UCSC Ensembl
chr1:102559204..102559204hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534513
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052904
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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