A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069940



Internal ID21462066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:19237572..19237664hg38UCSC Ensembl
chr10:19526501..19526593hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595705
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069940
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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