A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672085



Internal ID21620390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:18334928..18335219hg38UCSC Ensembl
chrX:18353048..18353339hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166555
SamplesNA20509
Known GenesSCML2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672085
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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