A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285826



Internal ID20495044
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 StatusS
Merged Variantsnsv4763231
Supporting Variants
Samples
Known GenesENTPD1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285826
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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