A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041540



Internal ID21950873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111123794..111123794hg38UCSC Ensembl
chr1:111666416..111666416hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381126
hg191126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17533119
Samples
Known GenesDRAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041540
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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