A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360669



Internal ID22586338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97131619..97131770hg38UCSC Ensembl
chr10:98891376..98891527hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924469
Supporting Variants
Samples
Known GenesSLIT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360669
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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