A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138355



Internal ID337539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52756964..52968964hg38UCSC Ensembl
chrX:52786041..52998153hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38212001
hg19212113
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv567n206
Supporting Variantsnssv17737000
Samples
Known GenesFAM156A, FAM156B, SPANXN5, SSX2, SSX2B, XAGE3, XAGE5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138355
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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