A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2802562



Internal ID21247900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66400522..66400522hg38UCSC Ensembl
chr1:66866205..66866205hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13691262, nssv13683331
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2802562
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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