A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589703



Internal ID21781746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29654205..29654409hg38UCSC Ensembl
chr10:29943134..29943338hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013194
Supporting Variants
Samples
Known GenesSVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589703
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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