A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17164695



Internal ID21453563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107152053..107152053hg38UCSC Ensembl
chrX:106395283..106395283hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610820
Supporting Variants
SamplesHG02011
Known GenesNUP62CL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17164695
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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