A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267813



Internal ID20834853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10935751..10936229hg38UCSC Ensembl
chr6:10935984..10936462hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563511
Supporting Variants
Samples
Known GenesSYCP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267813
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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