A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074892



Internal ID21438342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62277957..62278015hg38UCSC Ensembl
chr11:62045429..62045487hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596181
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074892
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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