A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537663



Internal ID20910998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224255341..224256215hg38UCSC Ensembl
chr1:224443043..224443917hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18249363
Samples
Known GenesNVL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537663
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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