A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875851



Internal ID22650810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48104938..48252190hg38UCSC Ensembl
chrX:47964322..48111625hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38147253
hg19147304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452408
Samples
Known GenesSPACA5, SPACA5B, SSX5, SSX6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875851
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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