A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166548



Internal ID21492752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:18262540..18262926hg38UCSC Ensembl
chrX:18280660..18281046hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665890
Supporting Variants
SamplesNA19238
Known GenesSCML2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166548
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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