A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077060



Internal ID21473946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:10240379..10258107hg38UCSC Ensembl
chr12:10392978..10410706hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3817729
hg1917729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592574
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077060
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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