A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108855



Internal ID22018088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52405520..52861028hg38UCSC Ensembl
chrX:52148663..52890057hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38455509
hg19741395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638543
Samples
Known GenesSPANXN5, SSX2, SSX2B, SSX7, SSX8, XAGE1A, XAGE1B, XAGE1C, XAGE1D, XAGE1E, XAGE2, XAGE2B, XAGE5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108855
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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