A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545968



Internal ID20919188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:236914798..236915443hg38UCSC Ensembl
chr1:237078098..237078743hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38646
hg19646
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250781
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545968
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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