A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040930



Internal ID21950268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150744469..150744469hg38UCSC Ensembl
chr1:150716945..150716945hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532557
Samples
Known GenesCTSS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040930
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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