A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887351



Internal ID22662343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85106847..85107333hg38UCSC Ensembl
chrX:84361853..84362339hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458730
Samples
Known GenesSATL1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887351
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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