A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5474484



Internal ID252143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97208766..97211751hg38UCSC Ensembl
chr10:98968523..98971508hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg382986
hg192986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037583
Samples
Known GenesARHGAP19-SLIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5474484
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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