A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165145



Internal ID21429640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:122435458..122435458hg38UCSC Ensembl
chrX:121569311..121569311hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610112
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165145
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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