A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2802602



Internal ID21247941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85154442..85154442hg38UCSC Ensembl
chr1:85620125..85620125hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13709963
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2802602
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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