A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085414



Internal ID21410509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97989297..97989361hg38UCSC Ensembl
chr12:98383075..98383139hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587908
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085414
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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