A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2809009



Internal ID21254347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196511959..196511959hg38UCSC Ensembl
chr3:196238830..196238830hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13707918
Samples
Known GenesC3orf43
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2809009
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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