A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978461



Internal ID22753396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:766752..782337hg38UCSC Ensembl
chrX:727487..743072hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3815586
hg1915586
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516756
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978461
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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