A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560861



Internal ID20933932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:134681295..134681833hg38UCSC Ensembl
chr6:135002433..135002971hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38539
hg19539
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560861
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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