A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015988



Internal ID21925331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97162615..97162944hg38UCSC Ensembl
chr10:98922372..98922701hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582653
Samples
Known GenesARHGAP19-SLIT1, SLIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015988
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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