A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2800446



Internal ID21245784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:121795802..121795802hg38UCSC Ensembl
chr1:121424254..121424254hg19UCSC Ensembl
Cytoband1p11.2
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13693573
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2800446
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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