A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062634



Internal ID21433022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20981555..20981616hg38UCSC Ensembl
chr1:21308048..21308109hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584436
Supporting Variants
SamplesHG00731
Known GenesEIF4G3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062634
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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