A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5418301



Internal ID197476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44533583..44568015hg38UCSC Ensembl
chrX:44392829..44427261hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3834433
hg1934433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736666
Samples
Known GenesFUNDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5418301
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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