A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046571



Internal ID21955808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166947324..166947324hg38UCSC Ensembl
chr1:166916561..166916561hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520689
Samples
Known GenesILDR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046571
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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