A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17060789



Internal ID21432248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151599280..151599519hg38UCSC Ensembl
chr1:151571756..151571995hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580464
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17060789
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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