A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571264



Internal ID20944335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:82103779..82756089hg38UCSC Ensembl
chr6:82813496..83465806hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38652311
hg19652311
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274755
Samples
Known GenesIBTK, TPBG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571264
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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