A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17585540



Internal ID21777583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5662602..5662602hg38UCSC Ensembl
chr10:5704565..5704565hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6090813
Supporting Variants
Samples
Known GenesASB13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17585540
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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