A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076703



Internal ID21457836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104398705..104398899hg38UCSC Ensembl
chr12:104792483..104792677hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591479
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076703
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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