A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061547



Internal ID21457490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165085195..165085919hg38UCSC Ensembl
chr1:165054432..165055156hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569027
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061547
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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