A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168907



Internal ID21492344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85135735..85135735hg38UCSC Ensembl
chrX:84390741..84390741hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5621134
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168907
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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