A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13705162



Internal ID21198362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40022914..40039149hg38UCSC Ensembl
chr21:41394841..41411076hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3816236
hg1916236
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2803910
Supporting Variants
SamplesCHM1
Known GenesDSCAM
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13705162
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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