A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564781



Internal ID20937852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:70597345..70598095hg38UCSC Ensembl
chr6:71307048..71307798hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38751
hg19751
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274011
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564781
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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