A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168047



Internal ID21500582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5288771..5288771hg38UCSC Ensembl
chrX:5206812..5206812hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620565
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168047
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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