A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072071



Internal ID21437042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97900573..97900573hg38UCSC Ensembl
chr10:99660330..99660330hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628206
Supporting Variants
SamplesHG00731
Known GenesCRTAC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072071
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