A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978492



Internal ID22753427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:79504102..79515738hg38UCSC Ensembl
chrX:78759599..78771235hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3811637
hg1911637
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516807
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978492
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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