A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586725



Internal ID20959796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33316529..33317281hg38UCSC Ensembl
chr11:33338075..33338827hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225101
Samples
Known GenesHIPK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586725
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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