A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576784



Internal ID20949855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32629837..32630107hg38UCSC Ensembl
chr11:32651383..32651653hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217804
Samples
Known GenesCCDC73
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576784
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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