A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516190



Internal ID22574152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37034423..37048270hg38UCSC Ensembl
chrX:37052496..37066343hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3813848
hg1913848
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974639
Supporting Variants
Samples
Known GenesFTH1P18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516190
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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