A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070942



Internal ID21436575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72064898..72065201hg38UCSC Ensembl
chr10:73824656..73824959hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592519
Supporting Variants
SamplesHG00731
Known GenesSPOCK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070942
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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