A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5493677



Internal ID270848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13730176..13732251hg38UCSC Ensembl
chr10:13772176..13774251hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382076
hg192076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030295
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5493677
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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