A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071047



Internal ID21483280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5771888..5772554hg38UCSC Ensembl
chr10:5813851..5814517hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38667
hg19667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586103
Supporting Variants
SamplesHG03732
Known GenesGDI2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071047
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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