A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549960



Internal ID20923111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:140333526..140333599hg38UCSC Ensembl
chr2:141091095..141091168hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253820
Samples
Known GenesLRP1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549960
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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