A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2814848



Internal ID21260186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26955702..26955702hg38UCSC Ensembl
chr7:26995321..26995321hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13706258, nssv13705129
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2814848
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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