A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044949



Internal ID21954219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11926481..11932290hg38UCSC Ensembl
chr1:143159072..143165618hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg385810
hg196547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044949
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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