A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071268



Internal ID21444201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67784403..67795563hg38UCSC Ensembl
chr10:69544161..69555321hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3811161
hg1911161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597233
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071268
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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