A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17077107



Internal ID21402774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:107686693..107687757hg38UCSC Ensembl
chr12:108080470..108081534hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381065
hg191065
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590042
Supporting Variants
SamplesHG00171
Known GenesPWP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17077107
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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