A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515084



Internal ID22573043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:105550635..105551698hg38UCSC Ensembl
chrX:104794628..104795691hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg381064
hg191064
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975036
Supporting Variants
Samples
Known GenesIL1RAPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515084
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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