A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068112



Internal ID21490771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22726632..22727824hg38UCSC Ensembl
chr10:23015561..23016753hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg381193
hg191193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589721
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068112
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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