A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976619



Internal ID22751554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100724252..100730731hg38UCSC Ensembl
chrX:99979233..99985719hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg386480
hg196487
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515040
Samples
Known GenesSYTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976619
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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