A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682654



Internal ID21204512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8539911..8539911hg38UCSC Ensembl
chr3:8581597..8581597hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807611
Supporting Variants
Samples
Known GenesLMCD1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682654
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.109375


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