A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084435



Internal ID21488091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:34194003..34194066hg38UCSC Ensembl
chr12:34346938..34347001hg19UCSC Ensembl
Cytoband12p11.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585578
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084435
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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