A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562375



Internal ID20935446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11125083..11126118hg38UCSC Ensembl
chr6:11125316..11126351hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg381036
hg191036
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6057n223
Supporting Variantsnssv18268486
Samples
Known GenesSMIM13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562375
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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