A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3935277



Internal ID21355347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65249084..65249138hg38UCSC Ensembl
chr11:65016555..65016609hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15181287
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3935277
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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