A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976318



Internal ID22751253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:105484159..105492027hg38UCSC Ensembl
chrX:104728151..104736019hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg387869
hg197869
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515083
Samples
Known GenesIL1RAPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976318
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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