A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553688



Internal ID20926799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229559627..229560349hg38UCSC Ensembl
chr1:229695374..229696096hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv549n223
Supporting Variantsnssv18250334
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553688
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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