A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119083



Internal ID21459900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33652044..33653058hg38UCSC Ensembl
chr21:35024350..35025364hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381015
hg191015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594156
Supporting Variants
SamplesHG02818
Known GenesITSN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119083
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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