A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2806071



Internal ID21251409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:202577539..202577539hg38UCSC Ensembl
chr2:203442262..203442262hg19UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13683780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2806071
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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