A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2800869



Internal ID21246207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150781535..150781535hg38UCSC Ensembl
chr1:150754011..150754011hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13695744
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2800869
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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