A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285277



Internal ID20494495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:54655227..54655284hg38UCSC Ensembl
chr10:56414987..56415044hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739665
Supporting Variants
Samples
Known GenesPCDH15
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285277
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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