A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536744



Internal ID20910087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:69536837..69548477hg38UCSC Ensembl
chr1:70002520..70014160hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3811641
hg1911641
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18251319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536744
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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