A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541500



Internal ID20914781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207401945..207402579hg38UCSC Ensembl
chr1:207575290..207575924hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250019
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541500
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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