A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166202



Internal ID21492815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21467682..21467682hg38UCSC Ensembl
chrX:21485800..21485800hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614542
Supporting Variants
SamplesNA19238
Known GenesCNKSR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166202
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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