A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138560



Internal ID337744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52480000..52714964hg38UCSC Ensembl
chrX:52223143..52744013hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38234965
hg19520871
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736990
Samples
Known GenesSSX2, SSX2B, SSX7, SSX8, XAGE1A, XAGE1B, XAGE1C, XAGE1D, XAGE1E, XAGE2, XAGE2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138560
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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