A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065649



Internal ID21491141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5667665..5667860hg38UCSC Ensembl
chr1:5727725..5727920hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583504
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065649
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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