A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790384



Internal ID21235722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3654798..3654798hg38UCSC Ensembl
chr11:3676028..3676028hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3817907
hg1917907
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687916
Samples
Known GenesART1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790384
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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