A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763231



Internal ID20539091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95986355..95986355hg38UCSC Ensembl
chr10:97746112..97746112hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285826
Samples
Known GenesENTPD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763231
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer