A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067457



Internal ID21490867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101819584..101819653hg38UCSC Ensembl
chr10:103579341..103579410hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585833
Supporting Variants
SamplesNA19238
Known GenesKCNIP2-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067457
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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