A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578534



Internal ID20951605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74131835..74131959hg38UCSC Ensembl
chr11:73842880..73843004hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236077
Samples
Known GenesC2CD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578534
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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