A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5973257



Internal ID22748192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119200104..119204727hg38UCSC Ensembl
chrX:118334067..118338690hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg384624
hg194624
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515245
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5973257
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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