A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2800475



Internal ID21245813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14514330..14514330hg38UCSC Ensembl
chr1:14840826..14840826hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13688015, nssv13691803
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2800475
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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