A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081644



Internal ID21990877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96025188..96025188hg38UCSC Ensembl
chr10:97784945..97784945hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592830
Samples
Known GenesCC2D2B, ENTPD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081644
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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