A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2807537



Internal ID21252875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45890319..45890319hg38UCSC Ensembl
chr3:45931811..45931811hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13685608
Samples
Known GenesCCR9, LZTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2807537
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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