A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556895



Internal ID20929966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99419559..99420236hg38UCSC Ensembl
chr6:99867435..99868112hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6335n223
Supporting Variantsnssv18272828
Samples
Known GenesPNISR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556895
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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