A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975630



Internal ID22750565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3277964..3283395hg38UCSC Ensembl
chrX:3196005..3201436hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg385432
hg195432
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516149
Samples
Known GenesCXorf28
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975630
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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