A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167595



Internal ID21446446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47148585..47148646hg38UCSC Ensembl
chrX:47007984..47008045hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669666
Supporting Variants
SamplesHG00732
Known GenesRBM10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167595
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer