A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071355



Internal ID21401424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86722513..86722819hg38UCSC Ensembl
chr10:88482270..88482576hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599573
Supporting Variants
SamplesHG00096
Known GenesLDB3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071355
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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