A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069861



Internal ID21402324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43599977..43600156hg38UCSC Ensembl
chr10:44095425..44095604hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601888
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069861
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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