A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601876



Internal ID21550528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1038879..1039004hg38UCSC Ensembl
chr10:1084819..1084944hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068493
SamplesHG00731
Known GenesIDI2-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601876
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