A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088647



Internal ID21459548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32655327..32655493hg38UCSC Ensembl
chr12:32808261..32808427hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597079
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088647
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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