A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072279



Internal ID21437128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95986358..95986358hg38UCSC Ensembl
chr10:97746115..97746115hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643208
Supporting Variants
SamplesHG00731
Known GenesENTPD1-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072279
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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