A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538604



Internal ID20911917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160918497..160919076hg38UCSC Ensembl
chr1:160888287..160888866hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247337
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538604
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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