A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2807611



Internal ID21252949
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 StatusM
Merged Variants
Supporting Variantsnssv13682654
Samples
Known GenesLMCD1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2807611
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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