A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974639



Internal ID22749574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37034423..37048270hg38UCSC Ensembl
chrX:37052496..37066343hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3813848
hg1913848
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516190
Samples
Known GenesFTH1P18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974639
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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