A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099715



Internal ID22008948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50076842..50076842hg38UCSC Ensembl
chr10:51836602..51836602hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17593547
Samples
Known GenesFAM21A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099715
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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