A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588107



Internal ID21780150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123999809..123999900hg38UCSC Ensembl
chr10:125759325..125759416hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6009417
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588107
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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