A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062407



Internal ID21491636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201032018..201032071hg38UCSC Ensembl
chr1:201001146..201001199hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5576414
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062407
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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