A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074876



Internal ID21438332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61867909..61868042hg38UCSC Ensembl
chr11:61635381..61635514hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596888
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074876
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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