A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073644



Internal ID21502623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:19533691..19534002hg38UCSC Ensembl
chr11:19555238..19555549hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587504
Supporting Variants
SamplesNA19239
Known GenesNAV2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073644
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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