A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271237



Internal ID20838277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34643022..34643711hg38UCSC Ensembl
chr6:34610799..34611488hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568880
Supporting Variants
Samples
Known GenesC6orf106
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271237
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00026


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