A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554951



Internal ID20928040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27239124..27239690hg38UCSC Ensembl
chr1:27565615..27566181hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252262
Samples
Known GenesWDTC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554951
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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