A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068367



Internal ID21503131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114647208..114647361hg38UCSC Ensembl
chr10:116406967..116407120hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593707
Supporting Variants
SamplesNA19239
Known GenesABLIM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068367
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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