A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072081



Internal ID21464990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98044322..98044572hg38UCSC Ensembl
chr10:99804079..99804329hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604005
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072081
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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