A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095580



Internal ID21458221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113625445..113625497hg38UCSC Ensembl
chr13:114279760..114279812hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599428
Supporting Variants
SamplesHG02587
Known GenesTFDP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095580
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