A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595325



Internal ID20968396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96039800..96042777hg38UCSC Ensembl
chr11:95772964..95775941hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382978
hg192978
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229656
Samples
Known GenesMAML2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595325
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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