A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589094



Internal ID21781137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6000959..6001132hg38UCSC Ensembl
chr10:6042922..6043095hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004030
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589094
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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