A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2816612



Internal ID21261950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:52166820..52166820hg38UCSC Ensembl
chr7:52234516..52234516hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13711063
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2816612
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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