A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274638



Internal ID20483856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78759075..78759435hg38UCSC Ensembl
chr10:80518832..80519192hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749459
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274638
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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