A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555558



Internal ID20928644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63170635..63171210hg38UCSC Ensembl
chr1:63636306..63636881hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250570
Samples
Known GenesLINC00466
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555558
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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