A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071336



Internal ID21476508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8023953..8025354hg38UCSC Ensembl
chr10:8065916..8067317hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592320
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071336
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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