A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2800400



Internal ID21245738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102093576..102093576hg38UCSC Ensembl
chr1:102559132..102559132hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13695873
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2800400
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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