A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2803456



Internal ID21248794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10129135..10129135hg38UCSC Ensembl
chr21:10607163..10607163hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13689481, nssv13694585
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2803456
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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