A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558574



Internal ID20931645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2998034..3056986hg38UCSC Ensembl
chr6:2998268..3057220hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3858953
hg1958953
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6046n223
Supporting Variantsnssv18270533
Samples
Known GenesHTATSF1P2, NQO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558574
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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