A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17364839



Internal ID22590508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:127739799..127740079hg38UCSC Ensembl
chr10:129538063..129538343hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5922154
Supporting Variants
Samples
Known GenesFOXI2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17364839
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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