A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965314



Internal ID22740250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95758002..95758002hg38UCSC Ensembl
chr10:97517759..97517759hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351459
Samples
Known GenesENTPD1, ENTPD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965314
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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