A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738031



Internal ID161697
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 StatusS
Merged Variantsnsv6138225
Supporting Variants
Samples
Known GenesMAGEA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738031
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00152711


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