A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538733



Internal ID20912047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21264457..21264975hg38UCSC Ensembl
chr1:21590950..21591468hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248518
Samples
Known GenesECE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538733
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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