A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17595212



Internal ID21787255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34482496..34514914hg38UCSC Ensembl
chr10:34771424..34803842hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3832419
hg1932419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009659
Supporting Variants
Samples
Known GenesPARD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17595212
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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