A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166657



Internal ID21508444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22412695..22412695hg38UCSC Ensembl
chrX:22430812..22430812hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620911
Supporting Variants
SamplesNA20509
Known GenesLOC100873065
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166657
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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