A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057578



Internal ID21966811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:117932522..117932522hg38UCSC Ensembl
chr1:118475145..118475145hg19UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533131
Samples
Known GenesWDR3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057578
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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