A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068359



Internal ID21447875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114101962..114102270hg38UCSC Ensembl
chr10:115861721..115862029hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597426
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068359
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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