A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062065



Internal ID21432787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19642973..19643116hg38UCSC Ensembl
chr1:19969467..19969610hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573535
Supporting Variants
SamplesHG00731
Known GenesMINOS1-NBL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062065
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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