A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6544707



Internal ID20917944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:217900597..217900722hg38UCSC Ensembl
chr1:218073939..218074064hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248638
Samples
Known GenesLINC00210
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6544707
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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