A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292609



Internal ID20501827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9786343..9796403hg38UCSC Ensembl
chr1:9846401..9856461hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3810061
hg1910061
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4746404
Supporting Variants
Samples
Known GenesCLSTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292609
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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