A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537671



Internal ID20911006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151275273..151275908hg38UCSC Ensembl
chr1:151247749..151248384hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38636
hg19636
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537671
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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