A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588337



Internal ID21780380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59498499..59498581hg38UCSC Ensembl
chr10:61258257..61258339hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013114
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588337
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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