A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554868



Internal ID20927958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62484500..62484969hg38UCSC Ensembl
chr1:62950171..62950640hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250547
Samples
Known GenesDOCK7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554868
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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