A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3945216



Internal ID21365285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11854051..11855011hg38UCSC Ensembl
chr11:11875598..11876558hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38961
hg19961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15181210
SamplesHG002
Known GenesUSP47
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3945216
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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