A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497618



Internal ID274646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125947502..125964000hg38UCSC Ensembl
chr10:127636071..127652569hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3816499
hg1916499
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038946
Samples
Known GenesFANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497618
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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