A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072002



Internal ID21403516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88155365..88155365hg38UCSC Ensembl
chr10:89915122..89915122hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642384
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072002
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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