A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543385



Internal ID20916633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40169370..40169957hg38UCSC Ensembl
chr1:40635042..40635629hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38588
hg19588
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250920
Samples
Known GenesRLF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543385
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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