A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138235



Internal ID337418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141698190..141935690hg38UCSC Ensembl
chrX:140786347..141023476hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38237501
hg19237130
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742754
Samples
Known GenesMAGEC1, MAGEC3, SPANXD, SPANXE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138235
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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