A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070690



Internal ID21481657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5307003..5308261hg38UCSC Ensembl
chr10:5348966..5350224hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg381259
hg191259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601259
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070690
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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