A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2801569



Internal ID21246907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227492580..227508781hg38UCSC Ensembl
chr1:227680281..227696482hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3816202
hg1916202
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13701118
SamplesCHM1
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2801569
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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