A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2815271



Internal ID21260609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137946951..137946951hg38UCSC Ensembl
chr7:137631697..137631697hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13702066
Samples
Known GenesCREB3L2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2815271
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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