A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166470



Internal ID21462945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:147901983..147904004hg38UCSC Ensembl
chrX:146983501..146985522hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg382022
hg192022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667734
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166470
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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