A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065722



Internal ID21443949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36740614..36740693hg38UCSC Ensembl
chr1:37206215..37206294hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571671
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065722
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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