A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082190



Internal ID21499322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100550321..100550416hg38UCSC Ensembl
chr13:101202575..101202670hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589117
Supporting Variants
SamplesNA19239
Known GenesGGACT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082190
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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