A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061606



Internal ID21476131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173688653..173688702hg38UCSC Ensembl
chr1:173657792..173657841hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5569136
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061606
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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