A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551942



Internal ID20925074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38901700..38902671hg38UCSC Ensembl
chr1:39367372..39368343hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38972
hg19972
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252422
Samples
Known GenesRHBDL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551942
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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