A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168718



Internal ID21408037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9061546..9061546hg38UCSC Ensembl
chrX:9029587..9029587hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604773
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168718
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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