A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368588



Internal ID22594257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125961505..125982297hg38UCSC Ensembl
chr10:127650074..127670866hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3820793
hg1920793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5924914
Supporting Variants
Samples
Known GenesFANK1, FANK1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368588
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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