A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545228



Internal ID20918461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:88623515..88623612hg38UCSC Ensembl
chr1:89089198..89089295hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251941
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545228
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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