A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536903



Internal ID20910247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224369530..224369698hg38UCSC Ensembl
chr1:224557232..224557400hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249374
Samples
Known GenesCNIH4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536903
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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