A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275963



Internal ID20485181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32195142..32197900hg38UCSC Ensembl
chr10:32484070..32486828hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg382759
hg192759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736861
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275963
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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