A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167000



Internal ID21446060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30571256..30571256hg38UCSC Ensembl
chrX:30589373..30589373hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614881
Supporting Variants
SamplesHG00732
Known GenesCXorf21
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167000
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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