A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927401



Internal ID22702629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17401838..17574972hg38UCSC Ensembl
chr10:17443837..17616971hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38173135
hg19173135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360265
Samples
Known GenesST8SIA6, ST8SIA6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927401
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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