A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600855



Internal ID21549498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31771728..31771830hg38UCSC Ensembl
chr17:30098747..30098849hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082338
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600855
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