A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569314



Internal ID20942385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4169872..4174777hg38UCSC Ensembl
chr6:4170106..4175011hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg384906
hg194906
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569314
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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