A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422287



Internal ID201333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136041515..136041574hg38UCSC Ensembl
chrX:135123674..135123733hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742522
Samples
Known GenesSLC9A6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422287
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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