A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570202



Internal ID20943273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41868909..41869479hg38UCSC Ensembl
chr6:41836647..41837217hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270945
Samples
Known GenesUSP49
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570202
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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