A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17104291



Internal ID21493744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35208551..35208686hg38UCSC Ensembl
chr19:35699454..35699589hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591081
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17104291
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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