A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970181



Internal ID22745116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155996730..156006609hg38UCSC Ensembl
chrX:155226395..155236274hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg389880
hg199880
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515856, nssv17515855, nssv17515854
Samples
Known GenesIL9R
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970181
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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