A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053853



Internal ID21963086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:41705012..41705012hg38UCSC Ensembl
chr1:42170683..42170683hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg383008
hg193008
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526577
Samples
Known GenesHIVEP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053853
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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