A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545723



Internal ID20918948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:85209420..85209921hg38UCSC Ensembl
chr1:85675103..85675604hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253931
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545723
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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