A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166149



Internal ID21445639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17502493..17502807hg38UCSC Ensembl
chrX:17520616..17520930hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668596
Supporting Variants
SamplesHG00732
Known GenesNHS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166149
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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