A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978998



Internal ID22753933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64109829..64125626hg38UCSC Ensembl
chrX:63329709..63345506hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3815798
hg1915798
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516541, nssv17516542
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978998
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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