A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552861



Internal ID20925982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160815059..160815680hg38UCSC Ensembl
chr1:160784849..160785470hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247333
Samples
Known GenesLY9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552861
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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