A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070192



Internal ID21464366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38058499..38058604hg38UCSC Ensembl
chr10:38347427..38347532hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591038
Supporting Variants
SamplesHG03065
Known GenesZNF33A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070192
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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