A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934436



Internal ID21354506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63319320..63319374hg38UCSC Ensembl
chr11:63086792..63086846hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15181830
SamplesHG002
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934436
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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