A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880646



Internal ID22655616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100724910..100774493hg38UCSC Ensembl
chrX:99979898..100029482hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3849584
hg1949585
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17445465
Samples
Known GenesSYTL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880646
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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