A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13701468



Internal ID21198426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26639336..26648754hg38UCSC Ensembl
chr1:26965827..26975245hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg389419
hg199419
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801806
Supporting Variants
SamplesCHM13
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13701468
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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