A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550984



Internal ID20924127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109038763..109039291hg38UCSC Ensembl
chr1:109581385..109581913hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38529
hg19529
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247288
Samples
Known GenesWDR47
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550984
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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