A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564947



Internal ID20938018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151381509..151382509hg38UCSC Ensembl
chr6:151702644..151703644hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18269379
Samples
Known GenesZBTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564947
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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