A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072069



Internal ID21508234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97900509..97900828hg38UCSC Ensembl
chr10:99660266..99660585hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591784
Supporting Variants
SamplesNA20509
Known GenesCRTAC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072069
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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