A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167429



Internal ID21415045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49316490..49316490hg38UCSC Ensembl
chrX:49172969..49172969hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622455
Supporting Variants
SamplesHG00514
Known GenesGAGE10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167429
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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