A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061230



Internal ID21457485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160933396..160933478hg38UCSC Ensembl
chr1:160903186..160903268hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570878
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061230
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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