A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166344



Internal ID21445742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:156021578..156022828hg38UCSC Ensembl
chrX:155251243..155252493hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381251
hg191251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670312
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166344
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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