A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977827



Internal ID22752762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154546527..154558726hg38UCSC Ensembl
chrX:153774742..153786941hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3812200
hg1912200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515694
Samples
Known GenesG6PD, IKBKG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977827
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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