A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138225



Internal ID337408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152695606..152701606hg38UCSC Ensembl
chrX:151864081..151870084hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386001
hg196004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738031
Samples
Known GenesMAGEA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138225
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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