A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166781



Internal ID21445956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:29333514..29333689hg38UCSC Ensembl
chrX:29351631..29351806hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666257
Supporting Variants
SamplesHG00732
Known GenesIL1RAPL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166781
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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