A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557123



Internal ID20930194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155897948..155898048hg38UCSC Ensembl
chr6:156219082..156219182hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270118
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557123
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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