A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537766



Internal ID20911101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37085263..37085632hg38UCSC Ensembl
chr3:37126754..37127123hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259987
Samples
Known GenesLRRFIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537766
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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