A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17062748



Internal ID21502033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206151215..206151618hg38UCSC Ensembl
chr1:206189712..206190115hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575845
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17062748
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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