A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17079324



Internal ID21489959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:19096509..19096636hg38UCSC Ensembl
chr12:19249443..19249570hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600683
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17079324
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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