A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061445



Internal ID21508067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180869406..180869686hg38UCSC Ensembl
chr1:180838542..180838822hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575859
Supporting Variants
SamplesNA20509
Known GenesXPR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061445
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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