A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070208



Internal ID21481530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38264798..38265675hg38UCSC Ensembl
chr10:38553726..38554603hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38878
hg19878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590382
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070208
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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