A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070466



Internal ID21450536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63088161..63092487hg38UCSC Ensembl
chr10:64847921..64852247hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg384327
hg194327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591375
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070466
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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