A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594610



Internal ID21786653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9215291..9215344hg38UCSC Ensembl
chr10:9257254..9257307hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003067
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594610
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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